A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136949



Internal ID20703989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107439919..107440337hg38UCSC Ensembl
chr6:107761123..107761541hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617367
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00149


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