A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519442



Internal ID15446735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36137349..36143569hg38UCSC Ensembl
Innerchr9:36137346..36143566hg19UCSC Ensembl
Innerchr9:36127346..36133566hg18UCSC Ensembl
Innerchr9:36127346..36133566hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg386221
hg196221
hg186221
hg176221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694329
Samples
Known GenesGLIPR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519442
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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