A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162457



Internal ID20729497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99941069..99945602hg38UCSC Ensembl
chr7:99538692..99543225hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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