A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275220



Internal ID20484438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57606184..57606184hg38UCSC Ensembl
chr1:58071856..58071856hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763085
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275220
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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