A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048934



Internal ID21958168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65673025..65673025hg38UCSC Ensembl
chr2:65900159..65900159hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048934
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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