A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524226



Internal ID15451519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:25253508..25296605hg38UCSC Ensembl
InnerchrX:25271625..25314722hg19UCSC Ensembl
InnerchrX:25181546..25224643hg18UCSC Ensembl
InnerchrX:25031282..25074379hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3843098
hg1943098
hg1843098
hg1743098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700114
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524226
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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