A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179203



Internal ID20746243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48705024..48802509hg38UCSC Ensembl
chr14:49174227..49271712hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3897486
hg1997486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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