A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211576



Internal ID20778616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65022901..65640764hg38UCSC Ensembl
chr4:65888619..66506482hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38617864
hg19617864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381087
Supporting Variants
Samples
Known GenesEPHA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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