A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026617



Internal ID18769149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392318..31482053hg38UCSC Ensembl
Innerchr6:31360095..31449830hg19UCSC Ensembl
Innerchr6:31468074..31557809hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3889736
hg1989736
hg1889736
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5943n100
Supporting Variantsnssv3655792, nssv3655791, nssv3655794, nssv3655793
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026617
Frequency
Sample Size29084
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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