A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038488



Internal ID21947831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25919529..25919892hg38UCSC Ensembl
chr15:26164676..26165039hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603181
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038488
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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