A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033801



Internal ID19123022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167194096..167247175hg38UCSC Ensembl
Innerchr6:167607584..167660663hg19UCSC Ensembl
Innerchr6:167527574..167580653hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853080
hg1953080
hg1853080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n100
Supporting Variantsnssv3655405
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)nsv1033801
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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