A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948595



Internal ID21368664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16408564..16408863hg38UCSC Ensembl
chr3:16450071..16450370hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178920
SamplesHG002
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948595
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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