A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518348



Internal ID15445641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128269753..128532424hg38UCSC Ensembl
InnerchrX:127403730..127666402hg19UCSC Ensembl
InnerchrX:127231411..127494083hg18UCSC Ensembl
InnerchrX:127129265..127391937hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38262672
hg19262673
hg18262673
hg17262673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695776
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518348
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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