A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626632



Internal ID15850165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8680359..8715086hg38UCSC Ensembl
Outerchr3:8678934..8725956hg38UCSC Ensembl
Innerchr3:8722045..8756772hg19UCSC Ensembl
Outerchr3:8720620..8767642hg19UCSC Ensembl
Innerchr3:8697045..8731772hg18UCSC Ensembl
Outerchr3:8695620..8742642hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3847023
hg1947023
hg1847023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511207
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626632
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer