A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034297



Internal ID21943640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25159031..25159272hg38UCSC Ensembl
chr15:25404178..25404419hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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