A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv964224



Internal ID16258180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67498428..67640202hg38UCSC Ensembl
Innerchr3:67548852..67690626hg19UCSC Ensembl
Innerchr3:67631542..67773316hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38141775
hg19141775
hg18141775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590561
Supporting Variants
Samples
Known GenesSUCLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv964224
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