A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024732



Internal ID21934075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999817..25999887hg38UCSC Ensembl
chr15:26244964..26245034hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610715
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024732
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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