A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524543



Internal ID15451836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116458613..116619653hg38UCSC Ensembl
InnerchrX:115589779..115753621hg19UCSC Ensembl
InnerchrX:115503807..115637649hg18UCSC Ensembl
InnerchrX:115401661..115535503hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38161041
hg19163843
hg18133843
hg17133843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv526n21
Supporting Variantsnssv700493
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524543
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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