A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020096



Internal ID20587136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62654801..62655183hg38UCSC Ensembl
chr14:63121519..63121901hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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