A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026211



Internal ID18768743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31394533..31506911hg38UCSC Ensembl
Innerchr6:31362310..31474688hg19UCSC Ensembl
Innerchr6:31470289..31582667hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38112379
hg19112379
hg18112379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5942n100
Supporting Variantsnssv3655880
Samples
Known GenesHCG26, HCP5, MICA, MICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026211
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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