A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135380



Internal ID20702420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110783884..110791308hg38UCSC Ensembl
chr6:111105087..111112511hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387425
hg197425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617531
Supporting Variants
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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