A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832704



Internal ID16126660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94673523..94686776hg38UCSC Ensembl
Innerchr14:95139860..95153113hg19UCSC Ensembl
Innerchr14:94209613..94222866hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3813254
hg1913254
hg1813254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565627
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)nssv832704
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