A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163639



Internal ID20730679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112926601..112928200hg38UCSC Ensembl
chr8:113938830..113940429hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418550
Supporting Variants
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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