A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117375



Internal ID20684415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52833910..52834727hg38UCSC Ensembl
chr4:53700077..53700894hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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