A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979499



Internal ID22754434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71045728..71045728hg38UCSC Ensembl
chr17:69041869..69041869hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979499
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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