A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691259



Internal ID18642854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103223965..103301007hg38UCSC Ensembl
Innerchr8:104236193..104313235hg19UCSC Ensembl
Innerchr8:104305369..104382411hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877043
hg1977043
hg1877043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017326
Supporting Variants
Samples
Known GenesBAALC, FZD6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691259
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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