A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515495



Internal ID15443106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:104435681..104480322hg38UCSC Ensembl
InnerchrX:103680362..103725003hg19UCSC Ensembl
InnerchrX:103567018..103611659hg18UCSC Ensembl
InnerchrX:103486507..103531148hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3844642
hg1944642
hg1844642
hg1744642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675067, nssv653318, nssv667515, nssv665351
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515495
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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