A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751575



Internal ID20527435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309423..168309423hg38UCSC Ensembl
chr6:168710103..168710103hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267439
Samples
Known GenesDACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751575
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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