A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757332



Internal ID19055613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103589003..104181980hg38UCSC Ensembl
Innerchr8:104601231..105194208hg19UCSC Ensembl
Innerchr8:104670407..105263384hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38592978
hg19592978
hg18592978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031195
Supporting Variants
Samples
Known GenesRIMS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757332
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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