A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149926



Internal ID20716966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114884652..114885066hg38UCSC Ensembl
chr7:114524707..114525121hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00252


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