A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167383



Internal ID20734423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14287612..14288049hg38UCSC Ensembl
chr8:14145121..14145558hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424267
Supporting Variants
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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