A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691309



Internal ID18989590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113234129..113277850hg38UCSC Ensembl
Innerchr8:114246358..114290079hg19UCSC Ensembl
Innerchr8:114315534..114359255hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3843722
hg1943722
hg1843722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027156
Supporting Variants
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691309
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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