A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232151



Internal ID20799191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54973201..54986900hg38UCSC Ensembl
chr6:54837999..54851698hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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