A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970241



Internal ID22745176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29380907..29380907hg38UCSC Ensembl
chr17:27707925..27707925hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970241
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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