A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520952



Internal ID15448245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:71666911..71859800hg38UCSC Ensembl
InnerchrX:70886761..71079650hg19UCSC Ensembl
InnerchrX:70803486..70996375hg18UCSC Ensembl
InnerchrX:70669782..70862671hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38192890
hg19192890
hg18192890
hg17192890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv516n21
Supporting Variantsnssv678444, nssv687424
Samples
Known GenesBCYRN1, CXorf49, CXorf49B, LINC00891, LOC100132741
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520952
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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