A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970259



Internal ID47501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140681553..140936446hg38UCSC Ensembl
chr6:141002690..141257583hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38254894
hg19254894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457841
Supporting Variants
Samples
Known GenesMIR4465
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970259
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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