A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694329



Internal ID15430981
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519442
Supporting Variants
Samples
Known GenesGLIPR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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