A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172737



Internal ID20739777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91029116..91045611hg38UCSC Ensembl
chr8:92041344..92057839hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3816496
hg1916496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435395
Supporting Variants
Samples
Known GenesTMEM55A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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