A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380340



Internal ID21037893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112771372..112799083hg38UCSC Ensembl
chr4:113692528..113720239hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3827712
hg1927712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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