A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933526



Internal ID21353595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56881031..56881031hg38UCSC Ensembl
chr17:54958392..54958392hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185023
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933526
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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