A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158482



Internal ID20725522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53818901..54053094hg38UCSC Ensembl
chr7:53886594..54120787hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38234194
hg19234194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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