A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168496



Internal ID20735536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49958235..49961313hg38UCSC Ensembl
chr8:50870795..50873873hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg383079
hg193079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428023
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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