A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372451



Internal ID21030004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6265417..6293830hg38UCSC Ensembl
chr4:6267144..6295557hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3828414
hg1928414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210924
Samples
Known GenesWFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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