A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704703



Internal ID15441355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90344261..90390435hg38UCSC Ensembl
Innerchr9:93106543..93152717hg19UCSC Ensembl
Innerchr9:92146363..92192537hg18UCSC Ensembl
Innerchr9:90186097..90232271hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3846175
hg1946175
hg1846175
hg1746175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528155
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704703
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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