A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040186



Internal ID20607226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39635203..39692930hg38UCSC Ensembl
chr18:37215167..37272894hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3857728
hg1957728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529947
Supporting Variants
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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