A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020850



Internal ID20587890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67262634..67263169hg38UCSC Ensembl
chr14:67729351..67729886hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491239
Supporting Variants
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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