A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765736



Internal ID20541596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96153069..96153069hg38UCSC Ensembl
chr1:96618625..96618625hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765736
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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