A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv831391



Internal ID16125347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83637715..83692990hg38UCSC Ensembl
Innerchr14:84104059..84159334hg19UCSC Ensembl
Innerchr14:83173812..83229087hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3855276
hg1955276
hg1855276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565374
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)nssv831391
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