A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161042



Internal ID20728082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84522546..84530331hg38UCSC Ensembl
chr7:84151862..84159647hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387786
hg197786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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