A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522600



Internal ID15103207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:153481028..153504044hg38UCSC Ensembl
InnerchrX:152746486..152769502hg19UCSC Ensembl
InnerchrX:152399680..152422696hg18UCSC Ensembl
InnerchrX:152267333..152290349hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3823017
hg1923017
hg1823017
hg1723017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705991
Samples
Known GenesBGN, HAUS7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522600
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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