A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266194



Internal ID20475412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57984175..57984175hg38UCSC Ensembl
chr1:58449847..58449847hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756809
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266194
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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