A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817528



Internal ID16111484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94711363..94712997hg38UCSC Ensembl
Innerchr13:95363617..95365251hg19UCSC Ensembl
Innerchr13:94161618..94163252hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381635
hg191635
hg181635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562761
Supporting Variants
Samples
Known GenesSOX21, SOX21-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817528
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer