A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945642



Internal ID21365712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892616..84892616hg38UCSC Ensembl
chr2:85119740..85119740hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187860
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945642
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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