A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017633



Internal ID19106850
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 StatusM
Merged Variants
Supporting Variantsnssv3657482
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)nsv1017633
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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