A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212977



Internal ID20780017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65717520..65718653hg38UCSC Ensembl
chr3:65703195..65704328hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370414
Supporting Variants
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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