A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121354



Internal ID20688394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99862101..99864000hg38UCSC Ensembl
chr4:100783258..100785157hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394796
Supporting Variants
Samples
Known GenesDAPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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