A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214763



Internal ID20781803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87765027..87774935hg38UCSC Ensembl
chr4:88686179..88696087hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg389909
hg199909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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