A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958004



Internal ID15905274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4000518..4107492hg38UCSC Ensembl
Innerchr3:4042202..4149176hg19UCSC Ensembl
Innerchr3:4017202..4124176hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38106975
hg19106975
hg18106975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589407
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)nssv958004
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