A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385282



Internal ID21042835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84885204..84890335hg38UCSC Ensembl
chr4:85806357..85811488hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg385132
hg195132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214738
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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