A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827611



Internal ID16121567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44609773..44742112hg38UCSC Ensembl
Innerchr14:45078976..45211315hg19UCSC Ensembl
Innerchr14:44148726..44281065hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38132340
hg19132340
hg18132340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564696
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)nssv827611
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