A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152955



Internal ID20719995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17385802..17691728hg38UCSC Ensembl
chr7:17425426..17731352hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38305927
hg19305927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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