A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212755



Internal ID20779795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158658715..158672237hg38UCSC Ensembl
chr4:159579867..159593389hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3813523
hg1913523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378262
Supporting Variants
Samples
Known GenesC4orf46, ETFDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212755
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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