A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232810



Internal ID20799851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56301789..56501430hg38UCSC Ensembl
chr6:56166587..56366228hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38199642
hg19199642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402552
Supporting Variants
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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