A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380102



Internal ID21037655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102829677..102834512hg38UCSC Ensembl
chr4:103750834..103755669hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384836
hg194836
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209447
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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