A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3658771



Internal ID18957052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:67120640..68118445hg38UCSC Ensembl
Innerchr6:67830533..68828337hg19UCSC Ensembl
Innerchr6:67887254..68885058hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38997806
hg19997805
hg18997805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027923
Supporting Variants
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)nssv3658771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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