A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628951



Internal ID21820998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44668355..44668355hg38UCSC Ensembl
chr17:42745723..42745723hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099352
Supporting Variants
Samples
Known GenesC17orf104
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628951
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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