A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028659



Internal ID18771190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31385552..31492443hg38UCSC Ensembl
Innerchr6:31353329..31460220hg19UCSC Ensembl
Innerchr6:31461308..31568199hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38106892
hg19106892
hg18106892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5942n100
Supporting Variantsnssv3655789
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)nsv1028659
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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