A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044149



Internal ID20611189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76007190..76007787hg38UCSC Ensembl
chr18:73719145..73719742hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00153


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