A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029871



Internal ID21939214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48943850..48943907hg38UCSC Ensembl
chr15:49236047..49236104hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601486
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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