A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631329



Internal ID21823376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8511029..8511029hg38UCSC Ensembl
chr17:8414347..8414347hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088434
Supporting Variants
Samples
Known GenesMYH10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631329
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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