A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562762



Internal ID16350171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94711363..94713127hg38UCSC Ensembl
Innerchr13:95363617..95365381hg19UCSC Ensembl
Innerchr13:94161618..94163382hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381765
hg191765
hg181765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3325n54
Supporting Variantsnssv817529
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)nsv562762
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