A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051264



Internal ID21960497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10399575..10399575hg38UCSC Ensembl
chr2:10539701..10539701hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535148
Samples
Known GenesHPCAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051264
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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