A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022441



Internal ID20589481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87741462..87792183hg38UCSC Ensembl
chr14:88207806..88258527hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850722
hg1950722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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