A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031894



Internal ID19121116
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 StatusM
Merged Variants
Supporting Variantsnssv3675916
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)nsv1031894
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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