A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192832



Internal ID20759872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81825701..81832100hg38UCSC Ensembl
chr14:82292045..82298444hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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