A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704441



Internal ID15441093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110636281..110641566hg38UCSC Ensembl
Innerchr9:113398561..113403846hg19UCSC Ensembl
Innerchr9:112438382..112443667hg18UCSC Ensembl
Innerchr9:110478116..110483401hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385286
hg195286
hg185286
hg175286
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527933
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704441
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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