A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373962



Internal ID21031515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86493066..86494268hg38UCSC Ensembl
chr3:86542216..86543418hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381203
hg191203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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