A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273625



Internal ID20482843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17030459..17030459hg38UCSC Ensembl
chr17:16933773..16933773hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273625
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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