A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520914



Internal ID15448207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86236694..86302046hg38UCSC Ensembl
Innerchr10:87996451..88061803hg19UCSC Ensembl
Innerchr10:87986431..88051783hg18UCSC Ensembl
Innerchr10:87986431..88051783hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3865353
hg1965353
hg1865353
hg1765353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697685
Samples
Known GenesGRID1, MIR346
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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