A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031938



Internal ID21941281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51914416..51914632hg38UCSC Ensembl
chr15:52206613..52206829hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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