A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657482



Internal ID18955763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54070538..54253678hg38UCSC Ensembl
Innerchr6:53935336..54118476hg19UCSC Ensembl
Innerchr6:54043295..54226435hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38183141
hg19183141
hg18183141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017633
Supporting Variants
Samples
Known GenesMLIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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