A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149939



Internal ID20716979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1150007..1158683hg38UCSC Ensembl
chr7:1189643..1198319hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg388677
hg198677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603008
Supporting Variants
Samples
Known GenesZFAND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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