A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932995



Internal ID21353064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223000371..223005159hg38UCSC Ensembl
chr2:223865089..223869877hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg384789
hg194789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178722
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932995
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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