A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767537



Internal ID20543397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170643312..170643312hg38UCSC Ensembl
chr1:170612453..170612453hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767537
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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