A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657647



Internal ID18955928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63316957..63392140hg38UCSC Ensembl
Innerchr6:64026862..64102045hg19UCSC Ensembl
Innerchr6:64084821..64160004hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3875184
hg1975184
hg1875184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031548
Supporting Variants
Samples
Known GenesLGSN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657647
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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