A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380037



Internal ID21037590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84885731..84886406hg38UCSC Ensembl
chr4:85806884..85807559hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119660
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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