A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261075



Internal ID20470293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137117198..137117737hg38UCSC Ensembl
chr6:137438335..137438874hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261075
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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