A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927482



Internal ID21347551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71855998..71856325hg38UCSC Ensembl
chr17:69852139..69852466hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176550
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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