A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171778



Internal ID20738818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94156319..94159963hg38UCSC Ensembl
chr8:95168547..95172191hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383645
hg193645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421389
Supporting Variants
Samples
Known GenesCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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