A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190367



Internal ID20757407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37633852..37634452hg38UCSC Ensembl
chr14:38103057..38103657hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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