A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926485



Internal ID21346554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195568480..195568529hg38UCSC Ensembl
chr2:196433204..196433253hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178427
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926485
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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