A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192535



Internal ID20759575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82928046..83480826hg38UCSC Ensembl
chr14:83394390..83947170hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38552781
hg19552781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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