A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038171



Internal ID21947514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35656608..35656712hg38UCSC Ensembl
chr15:35948809..35948913hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608538
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038171
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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