A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705470



Internal ID15095436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104919731..104920841hg38UCSC Ensembl
Innerchr9:107682012..107683122hg19UCSC Ensembl
Innerchr9:106721833..106722943hg18UCSC Ensembl
Innerchr9:104761567..104762677hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381111
hg191111
hg181111
hg171111
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528797
Supporting Variants
Samples
Known GenesABCA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705470
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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