A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053180



Internal ID21962413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58203392..58203392hg38UCSC Ensembl
chr1:58669064..58669064hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531610
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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