A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214739



Internal ID20781779
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 StatusS
Merged Variantsnsv6386359
Supporting Variants
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00107


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