A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv983573



Internal ID16277529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191343165..191352195hg38UCSC Ensembl
Innerchr3:191060954..191069984hg19UCSC Ensembl
Innerchr3:192543648..192552678hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg389031
hg199031
hg189031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592820
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)nssv983573
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