A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669398



Internal ID15059364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83611204..83638567hg38UCSC Ensembl
Innerchr9:86226119..86253482hg19UCSC Ensembl
Innerchr9:85415939..85443302hg18UCSC Ensembl
Innerchr9:83455673..83483036hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3827364
hg1927364
hg1827364
hg1727364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516587
Supporting Variants
Samples
Known GenesIDNK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669398
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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