A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383017



Internal ID21040570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86945569..87181189hg38UCSC Ensembl
chr4:87866721..88102341hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38235621
hg19235621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214757
Samples
Known GenesAFF1, KLHL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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