A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944003



Internal ID21364072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66712829..66712885hg38UCSC Ensembl
chr3:66763253..66763309hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179756
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944003
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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