A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044096



Internal ID20611137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8304153..8318807hg38UCSC Ensembl
chr18:8304151..8318805hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3814655
hg1914655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534367
Supporting Variants
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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