A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747085



Internal ID19045366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76292716..76318052hg38UCSC Ensembl
Innerchr6:77002433..77027769hg19UCSC Ensembl
Innerchr6:77059153..77084489hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3825337
hg1925337
hg1825337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030100
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)nssv3747085
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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