A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042063



Internal ID21951388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3671522..3671522hg38UCSC Ensembl
chr2:3719112..3719112hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519564
Samples
Known GenesALLC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042063
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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