A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195289



Internal ID20762329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91962793..91969021hg38UCSC Ensembl
chr14:92429137..92435365hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386229
hg196229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513535
Supporting Variants
Samples
Known GenesTRIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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