A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519679



Internal ID15446972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96535820..96579379hg38UCSC Ensembl
InnerchrX:95790819..95834378hg19UCSC Ensembl
InnerchrX:95677475..95721034hg18UCSC Ensembl
InnerchrX:95596964..95640523hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3843560
hg1943560
hg1843560
hg1743560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698961, nssv688981, nssv657545
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519679
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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