A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044194



Internal ID20611234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7646529..7820125hg38UCSC Ensembl
chr18:7646527..7820123hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38173597
hg19173597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516418
Supporting Variants
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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