A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152402



Internal ID20719442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142158945..142267110hg38UCSC Ensembl
chr7:141858745..141966928hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38108166
hg19108184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435520
Supporting Variants
Samples
Known GenesMOXD2P, PRSS58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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