A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526716



Internal ID15107323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:102582805..102934382hg38UCSC Ensembl
InnerchrX:101837733..102189310hg19UCSC Ensembl
InnerchrX:101724389..102075966hg18UCSC Ensembl
InnerchrX:101643878..101995455hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38351578
hg19351578
hg18351578
hg17351578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703056
Samples
Known GenesARMCX5, ARMCX5-GPRASP2, BHLHB9, GPRASP1, GPRASP2, LINC00630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526716
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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