A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527746



Internal ID15455039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:122088782..122179796hg38UCSC Ensembl
InnerchrX:121222635..121313649hg19UCSC Ensembl
InnerchrX:121050316..121141330hg18UCSC Ensembl
InnerchrX:120948170..121039184hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3891015
hg1991015
hg1891015
hg1791015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704232
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527746
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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