A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381760



Internal ID21039313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146126845..146128541hg38UCSC Ensembl
chr4:147047997..147049693hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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