A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518431



Internal ID15099038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26148083..26211140hg38UCSC Ensembl
Innerchr6:26148311..26211368hg19UCSC Ensembl
Innerchr6:26256290..26319347hg18UCSC Ensembl
Innerchr6:26256290..26319347hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3863058
hg1963058
hg1863058
hg1763058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv375n21
Supporting Variantsnssv694236
Samples
Known GenesHIST1H1E, HIST1H2AD, HIST1H2BD, HIST1H2BE, HIST1H2BF, HIST1H3D, HIST1H4D, HIST1H4E
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518431
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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