A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044752



Internal ID20611792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7729036..7761533hg38UCSC Ensembl
chr18:7729034..7761531hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3832498
hg1932498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524652
Supporting Variants
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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