A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158982



Internal ID20726022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79145139..79145488hg38UCSC Ensembl
chr7:78774455..78774804hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614197
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00224


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