A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701983



Internal ID15091949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30040354..30401268hg38UCSC Ensembl
Innerchr9:30040352..30401266hg19UCSC Ensembl
Innerchr9:30030352..30391266hg18UCSC Ensembl
Innerchr9:30030352..30391266hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38360915
hg19360915
hg18360915
hg17360915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known GenesLOC401497
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701983
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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