A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155214



Internal ID20722254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13853151..13879787hg38UCSC Ensembl
chr7:13892776..13919412hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3826637
hg1926637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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