A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv47n21



Internal ID22766239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80376908..80399783hg38UCSC Ensembl
chr10:82136664..82159539hg19UCSC Ensembl
chr10:82126644..82149519hg18UCSC Ensembl
chr10:82126644..82149519hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3822876
hg1922876
hg1822876
hg1722876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519314, nsv525264
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv47n21
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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