A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286244



Internal ID20495462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688482..36688482hg38UCSC Ensembl
chr1:37154083..37154083hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286244
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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