A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516804



Internal ID15444097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131439302..131454855hg38UCSC Ensembl
Innerchr10:133237565..133253118hg19UCSC Ensembl
Innerchr10:133127555..133143108hg18UCSC Ensembl
Innerchr10:133127555..133143108hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3815554
hg1915554
hg1815554
hg1715554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671041, nssv674521, nssv701274
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516804
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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