A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704434



Internal ID15094400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74504071..74549090hg38UCSC Ensembl
Innerchr9:77118987..77164006hg19UCSC Ensembl
Innerchr9:76308807..76353826hg18UCSC Ensembl
Innerchr9:74348541..74393560hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3845020
hg1945020
hg1845020
hg1745020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527927
Supporting Variants
Samples
Known GenesMIR6130, RORB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704434
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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