A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371009



Internal ID22596678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71439862..71439862hg38UCSC Ensembl
chr17:69436003..69436003hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371009
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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