A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013392



Internal ID22075023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8285313..8300183hg38UCSC Ensembl
Outerchr19:8270055..8313986hg38UCSC Ensembl
Innerchr19:8350197..8365067hg19UCSC Ensembl
Outerchr19:8334939..8378870hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3843932
hg1943932
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155549
Supporting Variants
Samples
Known GenesCD320, NDUFA7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013392
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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