A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519568



Internal ID15446861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:68993514..69051331hg38UCSC Ensembl
InnerchrX:68213357..68271174hg19UCSC Ensembl
InnerchrX:68130082..68187899hg18UCSC Ensembl
InnerchrX:67996378..68054195hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3857818
hg1957818
hg1857818
hg1757818
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701611, nssv656907, nssv692698, nssv692886
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519568
Frequency
Sample Size2026
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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