A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736571



Internal ID20512521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137778817..137778886hg38UCSC Ensembl
chr3:137497659..137497728hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736571
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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