A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527804



Internal ID15108411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116455651..116676857hg38UCSC Ensembl
InnerchrX:115586817..115810825hg19UCSC Ensembl
InnerchrX:115500845..115694853hg18UCSC Ensembl
InnerchrX:115398699..115592707hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38221207
hg19224009
hg18194009
hg17194009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704298
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527804
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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