A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437539



Internal ID15382845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23101028..23104563hg38UCSC Ensembl
Outerchr7:23096868..23108221hg38UCSC Ensembl
Innerchr7:23140647..23144182hg19UCSC Ensembl
Outerchr7:23136487..23147840hg19UCSC Ensembl
Innerchr7:23107172..23110707hg18UCSC Ensembl
Outerchr7:23103012..23114365hg18UCSC Ensembl
Innerchr7:22882919..22886454hg16UCSC Ensembl
Outerchr7:22878759..22890112hg16UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3811354
hg1911354
hg1811354
hg1611354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467420
SamplesNA18515
Known GenesKLHL7, KLHL7-AS1
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437539
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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