A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056698



Internal ID19145917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64564671..64631226hg38UCSC Ensembl
Innerchr16:64598574..64665129hg19UCSC Ensembl
Innerchr16:63156075..63222630hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3866556
hg1966556
hg1866556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559434, nssv3559433
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056698
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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