A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634819



Internal ID21826866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78419868..78419868hg38UCSC Ensembl
chr17:76415949..76415949hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087914
Supporting Variants
Samples
Known GenesPGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634819
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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