A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046156



Internal ID21955401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74061602..74061602hg38UCSC Ensembl
chr2:74288729..74288729hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517546
Samples
Known GenesTET3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046156
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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