A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377821



Internal ID21035374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149946614..150062354hg38UCSC Ensembl
chr4:150867766..150983506hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38115741
hg19115741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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