A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378262



Internal ID21035815
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 StatusM
Merged Variants
Supporting Variantsnssv18212755
Samples
Known GenesC4orf46, ETFDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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