A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689502



Internal ID18987783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:68530239..68574621hg38UCSC Ensembl
Innerchr8:69442474..69486856hg19UCSC Ensembl
Innerchr8:69605028..69649410hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3844383
hg1944383
hg1844383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023815
Supporting Variants
Samples
Known GenesC8orf34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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