A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022939



Internal ID19112156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137056586..137102642hg38UCSC Ensembl
Innerchr6:137377723..137423779hg19UCSC Ensembl
Innerchr6:137419416..137465472hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3846057
hg1946057
hg1846057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6151n100
Supporting Variantsnssv3654409
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)nsv1022939
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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