A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937386



Internal ID21357455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26251066..26251066hg38UCSC Ensembl
chr2:26473934..26473934hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187816
SamplesHG002
Known GenesHADHB
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937386
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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