A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654792



Internal ID18953073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14640318..14653295hg38UCSC Ensembl
Innerchr6:14640549..14653526hg19UCSC Ensembl
Innerchr6:14748528..14761505hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3812978
hg1912978
hg1812978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032949
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)nssv3654792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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