A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030490



Internal ID19119709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76730151..76758202hg38UCSC Ensembl
Innerchr6:77439868..77467919hg19UCSC Ensembl
Innerchr6:77496587..77524638hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3828052
hg1928052
hg1828052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3747158, nssv3659039, nssv3659035, nssv3659038, nssv3659036, nssv3659040, nssv3747157, nssv3659037, nssv3747156
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)nsv1030490
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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