A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031195



Internal ID19120416
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 StatusM
Merged Variants
Supporting Variantsnssv3757332
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)nsv1031195
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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