A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519163



Internal ID15099770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135553919..135691377hg38UCSC Ensembl
InnerchrX:134687844..134825092hg19UCSC Ensembl
InnerchrX:134515510..134652758hg18UCSC Ensembl
InnerchrX:134413364..134550612hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38137459
hg19137249
hg18137249
hg17137249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv531n21
Supporting Variantsnssv696645
Samples
Known GenesDDX26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519163
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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