A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359243



Internal ID21016796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57286390..57286465hg38UCSC Ensembl
chr3:57320418..57320493hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103500
Samples
Known GenesASB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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