A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372462



Internal ID21030015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2381642..2427659hg38UCSC Ensembl
chr4:2383369..2429386hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3846018
hg1946018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211775
Samples
Known GenesLOC402160, ZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372462
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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