A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045794



Internal ID20612834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79160418..79171364hg38UCSC Ensembl
chr18:76920418..76931364hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3810947
hg1910947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524807
Supporting Variants
Samples
Known GenesATP9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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