A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963361



Internal ID16257317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55800843..55842076hg38UCSC Ensembl
Innerchr3:55834871..55876104hg19UCSC Ensembl
Innerchr3:55809911..55851144hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3841234
hg1941234
hg1841234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590361
Supporting Variants
Samples
Known GenesERC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963361
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