A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522347



Internal ID8416622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119669316..119673412hg38UCSC Ensembl
Innerchr10:121428828..121432924hg19UCSC Ensembl
Innerchr10:121418818..121422914hg18UCSC Ensembl
Innerchr10:121418818..121422914hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384097
hg194097
hg184097
hg174097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695127
Samples
Known GenesBAG3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522347
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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