A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363544



Internal ID21021097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62511201..62548600hg38UCSC Ensembl
chr3:62496876..62534275hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3837400
hg1937400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4892n223
Supporting Variantsnssv18101774
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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