A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523507



Internal ID15450800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97602569..97688167hg38UCSC Ensembl
InnerchrX:96857568..96943166hg19UCSC Ensembl
InnerchrX:96744224..96829822hg18UCSC Ensembl
InnerchrX:96663713..96749311hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3885599
hg1985599
hg1885599
hg1785599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699278
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523507
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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