A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112440



Internal ID20679480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174362405..174362747hg38UCSC Ensembl
chr4:175283556..175283898hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00266


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