A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027535



Internal ID21936878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40683366..40683489hg38UCSC Ensembl
chr15:40975564..40975687hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027535
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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