A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931171



Internal ID21351240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21158293..21158293hg38UCSC Ensembl
chr2:21381165..21381165hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187090
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931171
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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