A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528256



Internal ID15108863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35557209..35628742hg38UCSC Ensembl
Innerchr9:35557206..35628739hg19UCSC Ensembl
Innerchr9:35547206..35618739hg18UCSC Ensembl
Innerchr9:35547206..35618739hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3871534
hg1971534
hg1871534
hg1771534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704822
Samples
Known GenesCD72, FAM166B, MIR4667, RUSC2, TESK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528256
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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