A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386359



Internal ID21043912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84962901..84965900hg38UCSC Ensembl
chr4:85884054..85887053hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214739
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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