A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184107



Internal ID20751147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73002815..73094054hg38UCSC Ensembl
chr14:73469523..73560762hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3891240
hg1991240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478629
Supporting Variants
Samples
Known GenesRBM25, ZFYVE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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