A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374648



Internal ID21032201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62541583..62542077hg38UCSC Ensembl
chr3:62527258..62527752hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101782
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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