A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365738



Internal ID21023291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62564032..62564637hg38UCSC Ensembl
chr3:62549707..62550312hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101784
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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