A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695388



Internal ID15432040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7789577..7790940hg38UCSC Ensembl
Innerchr9:7789577..7790940hg19UCSC Ensembl
Innerchr9:7779577..7780940hg18UCSC Ensembl
Innerchr9:7779577..7780940hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381364
hg191364
hg181364
hg171364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517976
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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