A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652736



Internal ID15042702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127870863..127871154hg38UCSC Ensembl
Innerchr9:130633142..130633433hg19UCSC Ensembl
Innerchr9:129672963..129673254hg18UCSC Ensembl
Innerchr9:127712696..127712987hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
hg17292
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517661
Supporting Variants
Samples
Known GenesAK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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