A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648988



Internal ID18947269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94040460..94496222hg38UCSC Ensembl
Innerchr6:94750178..95205940hg19UCSC Ensembl
Innerchr6:94806899..95262661hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38455763
hg19455763
hg18455763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022776
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)nssv3648988
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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