A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029757



Internal ID21939100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70212243..70213703hg38UCSC Ensembl
chr15:70504582..70506042hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029757
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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