A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699473



Internal ID15436125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144671047..144782779hg38UCSC Ensembl
InnerchrX:143752568..143864300hg19UCSC Ensembl
InnerchrX:143560125..143671997hg18UCSC Ensembl
InnerchrX:143457979..143569851hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38111733
hg19111733
hg18111873
hg17111873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523671
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699473
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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