A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528538



Internal ID15455831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88985208..89008952hg38UCSC Ensembl
InnerchrX:88240209..88263953hg19UCSC Ensembl
InnerchrX:88126865..88150609hg18UCSC Ensembl
InnerchrX:88046354..88070098hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3823745
hg1923745
hg1823745
hg1723745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705150
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528538
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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