A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211920



Internal ID20778960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53605162..53674409hg38UCSC Ensembl
chr4:54471329..54540576hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3869248
hg1969248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395002
Supporting Variants
Samples
Known GenesLNX1-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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