A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv983581



Internal ID16277537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191346739..191353021hg38UCSC Ensembl
Innerchr3:191064528..191070810hg19UCSC Ensembl
Innerchr3:192547222..192553504hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386283
hg196283
hg186283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592826
Supporting Variants
Samples
Known GenesCCDC50
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv983581
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