A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261380



Internal ID20470598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85277441..85277441hg38UCSC Ensembl
chr1:85743124..85743124hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759951
Supporting Variants
Samples
Known GenesLOC646626
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261380
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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