A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807251



Internal ID16101207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31954821..31962238hg38UCSC Ensembl
Innerchr13:32528958..32536375hg19UCSC Ensembl
Innerchr13:31426958..31434375hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg387418
hg197418
hg187418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561402
Supporting Variants
Samples
Known GenesEEF1DP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807251
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