A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034602



Internal ID21943945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25306771..25306961hg38UCSC Ensembl
chr15:25551918..25552108hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034602
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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