A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159989



Internal ID20727029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92523534..92527963hg38UCSC Ensembl
chr7:92152848..92157277hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg384430
hg194430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619519
Supporting Variants
Samples
Known GenesPEX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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