A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936653



Internal ID21356722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104947174..104947174hg38UCSC Ensembl
chr2:105563632..105563632hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187876
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936653
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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