A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382831



Internal ID21040384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158657968..158695765hg38UCSC Ensembl
chr4:159579120..159616917hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3837798
hg1937798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212754
Samples
Known GenesC4orf46, ETFDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382831
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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