A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053664



Internal ID21962897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69956477..69956477hg38UCSC Ensembl
chr2:70183609..70183609hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053664
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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