A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089378



Internal ID15942564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85565000..85628825hg38UCSC Ensembl
Innerchr7:85194316..85258141hg19UCSC Ensembl
Innerchr7:85032252..85096077hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3863826
hg1963826
hg1863826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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