A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957198



Internal ID22732338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56660987..56660987hg38UCSC Ensembl
chr6:56525785..56525785hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435368
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957198
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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