A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648972



Internal ID18947253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92656219..93006165hg38UCSC Ensembl
Innerchr6:93365937..93715883hg19UCSC Ensembl
Innerchr6:93422658..93772604hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38349947
hg19349947
hg18349947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031496
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)nssv3648972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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