A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618013



Internal ID21810060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12874207..12874263hg38UCSC Ensembl
chr18:12874206..12874262hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028129
Supporting Variants
Samples
Known GenesPTPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618013
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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