A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161177



Internal ID20728217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85363391..85363797hg38UCSC Ensembl
chr7:84992707..84993113hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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