A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677934



Internal ID15414586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78432975..78442493hg38UCSC Ensembl
Innerchr9:81047891..81057409hg19UCSC Ensembl
Innerchr9:80237711..80247229hg18UCSC Ensembl
Innerchr9:78277445..78286963hg17UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389519
hg199519
hg189519
hg179519
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515900
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677934
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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