A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526095



Internal ID15106702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29866264..29891740hg38UCSC Ensembl
Innerchr6:29834041..29859517hg19UCSC Ensembl
Innerchr6:29942020..29967496hg18UCSC Ensembl
Innerchr6:29942020..29967496hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3825477
hg1925477
hg1825477
hg1725477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702343
Samples
Known GenesHLA-H
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526095
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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