A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634589



Internal ID21826636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73716530..73716530hg38UCSC Ensembl
chr17:71712669..71712669hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634589
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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