A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436964



Internal ID15383205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120030051..120031798hg38UCSC Ensembl
Outerchr4:120025745..120043032hg38UCSC Ensembl
Innerchr4:120951206..120952953hg19UCSC Ensembl
Outerchr4:120946900..120964187hg19UCSC Ensembl
Innerchr4:121170654..121172401hg18UCSC Ensembl
Outerchr4:121166348..121183635hg18UCSC Ensembl
Innerchr4:121410025..121411772hg16UCSC Ensembl
Outerchr4:121405719..121423006hg16UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3817288
hg1917288
hg1817288
hg1617288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466845
SamplesNA10831
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)nsv436964
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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