A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274968



Internal ID20484186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37102849..37102849hg38UCSC Ensembl
chr1:37568450..37568450hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274968
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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