A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518671



Internal ID15445964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126978786..127429105hg38UCSC Ensembl
InnerchrX:126112769..126563086hg19UCSC Ensembl
InnerchrX:125940450..126390767hg18UCSC Ensembl
InnerchrX:125838304..126288621hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38450320
hg19450318
hg18450318
hg17450318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696121
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518671
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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