A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653272



Internal ID15389924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:146368360..146458610hg38UCSC Ensembl
InnerchrX:145449878..145540128hg19UCSC Ensembl
InnerchrX:145257570..145347820hg18UCSC Ensembl
InnerchrX:145155424..145245674hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3890251
hg1990251
hg1890251
hg1790251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653272
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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