A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520617



Internal ID15447910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126206455..126224963hg38UCSC Ensembl
InnerchrX:125340438..125358946hg19UCSC Ensembl
InnerchrX:125168119..125186627hg18UCSC Ensembl
InnerchrX:125065973..125084481hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3818509
hg1918509
hg1818509
hg1718509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691200, nssv673272
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520617
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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