A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675916



Internal ID18974197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16084388..16157888hg38UCSC Ensembl
Innerchr8:15941897..16015397hg19UCSC Ensembl
Innerchr8:15986268..16059768hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3873501
hg1973501
hg1873501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031894
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675916
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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