A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694690



Internal ID15431342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85302543..85303613hg38UCSC Ensembl
Innerchr9:87917458..87918528hg19UCSC Ensembl
Innerchr9:87107278..87108348hg18UCSC Ensembl
Innerchr9:85147012..85148082hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381071
hg191071
hg181071
hg171071
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521920
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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