A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522409



Internal ID15449702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120753323..120770626hg38UCSC Ensembl
Innerchr10:122512835..122530138hg19UCSC Ensembl
Innerchr10:122502825..122520128hg18UCSC Ensembl
Innerchr10:122502825..122520128hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3817304
hg1917304
hg1817304
hg1717304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695191
Samples
Known GenesMIR5694, WDR11-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522409
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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