A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365370



Internal ID21022923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58240883..58245314hg38UCSC Ensembl
chr3:58226610..58231041hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg384432
hg194432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212291
Samples
Known GenesABHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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