A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023909



Internal ID19113126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76730151..76759367hg38UCSC Ensembl
Innerchr6:77439868..77469084hg19UCSC Ensembl
Innerchr6:77496587..77525803hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3829217
hg1929217
hg1829217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3659048, nssv3659047
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)nsv1023909
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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