A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383730



Internal ID21041283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141426570..141492038hg38UCSC Ensembl
chr4:142347724..142413191hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3865469
hg1965468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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