A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259931



Internal ID20469149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8746826..8746826hg38UCSC Ensembl
chr17:8650144..8650144hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259931
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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