A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524521



Internal ID15451814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142252682..142282326hg38UCSC Ensembl
InnerchrX:141340468..141370112hg19UCSC Ensembl
InnerchrX:141168134..141197778hg18UCSC Ensembl
InnerchrX:141065988..141095632hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3829645
hg1929645
hg1829645
hg1729645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv534n21
Supporting Variantsnssv700469
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524521
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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