A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740497



Internal ID20516473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1530538..1530858hg38UCSC Ensembl
chr1:1465918..1466238hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268680
Samples
Known GenesATAD3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740497
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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