A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168730



Internal ID20735770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61467001..61474800hg38UCSC Ensembl
chr8:62379560..62387359hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424556
Supporting Variants
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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