A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992890



Internal ID20559930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7173091..7175033hg38UCSC Ensembl
chr11:7194322..7196264hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381943
hg191943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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