A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525819



Internal ID15106426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82442477..83021740hg38UCSC Ensembl
InnerchrX:81697926..82276748hg19UCSC Ensembl
InnerchrX:81584582..82163404hg18UCSC Ensembl
InnerchrX:81504071..82082893hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38579264
hg19578823
hg18578823
hg17578823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702005
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525819
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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