A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519525



Internal ID15446818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:86770824..86842588hg38UCSC Ensembl
InnerchrX:86025827..86097591hg19UCSC Ensembl
InnerchrX:85912483..85984247hg18UCSC Ensembl
InnerchrX:85831972..85903736hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3871765
hg1971765
hg1871765
hg1771765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694333
Samples
Known GenesDACH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519525
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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