A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701909



Internal ID15438561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18312580..18359016hg38UCSC Ensembl
Innerchr9:18312578..18359014hg19UCSC Ensembl
Innerchr9:18302578..18349014hg18UCSC Ensembl
Innerchr9:18302578..18349014hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3846437
hg1946437
hg1846437
hg1746437
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525743
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701909
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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