A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698878



Internal ID15435530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:71666911..71890381hg38UCSC Ensembl
InnerchrX:70886761..71110231hg19UCSC Ensembl
InnerchrX:70803486..71026956hg18UCSC Ensembl
InnerchrX:70669782..70893252hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38223471
hg19223471
hg18223471
hg17223471
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523166
Supporting Variants
Samples
Known GenesBCYRN1, CXorf49, CXorf49B, LINC00891, LOC100132741
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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