A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701429



Internal ID15438081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17591832..17618050hg38UCSC Ensembl
Innerchr9:17591830..17618048hg19UCSC Ensembl
Innerchr9:17581830..17608048hg18UCSC Ensembl
Innerchr9:17581830..17608048hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3826219
hg1926219
hg1826219
hg1726219
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517380
Supporting Variants
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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