A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927361



Internal ID21347430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73269132..73269132hg38UCSC Ensembl
chr17:71265271..71265271hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185054
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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