A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058903



Internal ID21968136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74840119..74840119hg38UCSC Ensembl
chr2:75067246..75067246hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535479
Samples
Known GenesHK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058903
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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