A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954378



Internal ID21374448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11166706..11166808hg38UCSC Ensembl
chr3:11208392..11208494hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179157
SamplesHG002
Known GenesHRH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954378
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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