A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752626



Internal ID20528486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56660996..56660996hg38UCSC Ensembl
chr6:56525794..56525794hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275385
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752626
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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