A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526800



Internal ID15454093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:143780400..143871047hg38UCSC Ensembl
InnerchrX:142863495..142954139hg19UCSC Ensembl
InnerchrX:142691161..142781805hg18UCSC Ensembl
InnerchrX:142589015..142679659hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3890648
hg1990645
hg1890645
hg1790645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703154
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526800
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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