A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362913



Internal ID21020466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128271543..128360009hg38UCSC Ensembl
chr3:127990386..128078852hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3888467
hg1988467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094132
Samples
Known GenesEEFSEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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