A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387891



Internal ID22445761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70738602..70738602hg38UCSC Ensembl
chr17:68734743..68734743hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972507
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387891
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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