A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522592



Internal ID8416867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43079488..43120057hg38UCSC Ensembl
Innerchr10:43574936..43615505hg19UCSC Ensembl
Innerchr10:42894942..42935511hg18UCSC Ensembl
Innerchr10:42894942..42935511hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3840570
hg1940570
hg1840570
hg1740570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705982
Samples
Known GenesRET
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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