A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356313



Internal ID21013866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128240839..128242608hg38UCSC Ensembl
chr3:127959682..127961451hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094131
Samples
Known GenesEEFSEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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