A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016501



Internal ID20583541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101245268..101404689hg38UCSC Ensembl
chr14:101711605..101871026hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159422
hg19159422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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