A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526612



Internal ID15107219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:2782116..2929092hg38UCSC Ensembl
InnerchrX:2700157..2847133hg19UCSC Ensembl
InnerchrX:2710157..2857133hg18UCSC Ensembl
InnerchrX:2693518..2840494hg17UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38146977
hg19146977
hg18146977
hg17146977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702932
Samples
Known GenesARSD, GYG2, XG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer