A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196987



Internal ID20764027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36055242..36068620hg38UCSC Ensembl
chr14:36524448..36537826hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3813379
hg1913379
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196987
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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