A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997639



Internal ID18810489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91267468..91336440hg38UCSC Ensembl
Innerchr4:92188619..92257591hg19UCSC Ensembl
Innerchr4:92407642..92476614hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3868973
hg1968973
hg1868973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5337n100
Supporting Variantsnssv3630957, nssv3630958
Samples
Known GenesCCSER1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997639
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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