A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963499



Internal ID16257455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61370576..61420153hg38UCSC Ensembl
Innerchr3:61356250..61405827hg19UCSC Ensembl
Innerchr3:61331290..61380867hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3849578
hg1949578
hg1849578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590426
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)nssv963499
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