A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962984



Internal ID15910254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449685..47451772hg38UCSC Ensembl
Innerchr3:47491175..47493262hg19UCSC Ensembl
Innerchr3:47466179..47468266hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382088
hg192088
hg182088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590229
Supporting Variants
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962984
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