A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158057



Internal ID20725097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67184785..67442036hg38UCSC Ensembl
chr7:66649772..66907023hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38257252
hg19257252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604589
Supporting Variants
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4, TYW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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