A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524712



Internal ID15452005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145221633..145237657hg38UCSC Ensembl
InnerchrX:144303153..144319177hg19UCSC Ensembl
InnerchrX:144110845..144126869hg18UCSC Ensembl
InnerchrX:144008699..144024723hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3816025
hg1916025
hg1816025
hg1716025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv536n21
Supporting Variantsnssv700697
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524712
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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