A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049626



Internal ID21958859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58241293..58241293hg38UCSC Ensembl
chr1:58706965..58706965hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522820
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049626
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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