A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161360



Internal ID20728400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100639383..100645523hg38UCSC Ensembl
chr8:101651611..101657751hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386141
hg196141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432141
Supporting Variants
Samples
Known GenesSNX31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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