A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023611



Internal ID21932954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41382984..41383111hg38UCSC Ensembl
chr15:41675182..41675309hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023611
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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