A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212126



Internal ID20779166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154679237..154686543hg38UCSC Ensembl
chr4:155600389..155607695hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387307
hg197307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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