A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383571



Internal ID21041124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102496301..102501000hg38UCSC Ensembl
chr4:103417458..103422157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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