A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379465



Internal ID21037018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94690678..94735278hg38UCSC Ensembl
chr4:95611829..95656429hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3844601
hg1944601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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