A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357643



Internal ID21015196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158599701..158601100hg38UCSC Ensembl
chr3:158317490..158318889hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094631
Samples
Known GenesMLF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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