A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559081



Internal ID21883436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997610..166997850hg38UCSC Ensembl
chr6:167411098..167411338hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013587
Supporting Variants
Samples
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559081
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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