A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437536



Internal ID15382842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13065384..13072698hg38UCSC Ensembl
Outerchr7:13060410..13112537hg38UCSC Ensembl
Innerchr7:13105009..13112323hg19UCSC Ensembl
Outerchr7:13100035..13152162hg19UCSC Ensembl
Innerchr7:13071534..13078848hg18UCSC Ensembl
Outerchr7:13066560..13118687hg18UCSC Ensembl
Innerchr7:12849346..12856660hg16UCSC Ensembl
Outerchr7:12844372..12896499hg16UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3852128
hg1952128
hg1852128
hg1652128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467417
SamplesNA18500
Known Genes
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)nsv437536
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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