A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624455



Internal ID15847991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58815172..58821732hg38UCSC Ensembl
Outerchr3:58814270..58831876hg38UCSC Ensembl
Innerchr3:58800898..58807458hg19UCSC Ensembl
Outerchr3:58799996..58817602hg19UCSC Ensembl
Innerchr3:58775938..58782498hg18UCSC Ensembl
Outerchr3:58775036..58792642hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3817607
hg1917607
hg1817607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511230
Supporting Variants
Samples1
Known GenesC3orf67
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624455
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