A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970099



Internal ID47393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136379347..136379398hg38UCSC Ensembl
chr6:136700485..136700536hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394061
Supporting Variants
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970099
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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