A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023505



Internal ID18766038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17386664..17451978hg38UCSC Ensembl
Innerchr6:17386895..17452209hg19UCSC Ensembl
Innerchr6:17494874..17560188hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3865315
hg1965315
hg1865315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5921n100
Supporting Variantsnssv3654806
Samples
Known GenesCAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023505
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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