A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517876



Internal ID15098483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14971199..15158964hg38UCSC Ensembl
Innerchr7:15010824..15198589hg19UCSC Ensembl
Innerchr7:14977349..15165114hg18UCSC Ensembl
Innerchr7:14784064..14971829hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38187766
hg19187766
hg18187766
hg17187766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695283
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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