A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029662



Internal ID21939005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77450559..77450646hg38UCSC Ensembl
chr15:77742901..77742988hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609760
Samples
Known GenesHMG20A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029662
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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