A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021815



Internal ID19111033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113382365..113478754hg38UCSC Ensembl
Innerchr6:113703567..113799956hg19UCSC Ensembl
Innerchr6:113810260..113906649hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3896390
hg1996390
hg1896390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6138n100
Supporting Variantsnssv3749514, nssv3749513, nssv3654306
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)nsv1021815
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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