A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816000



Internal ID16109956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81930550..82033775hg38UCSC Ensembl
Innerchr13:82504685..82607910hg19UCSC Ensembl
Innerchr13:81402686..81505911hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38103226
hg19103226
hg18103226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562451
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv816000
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