A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037472



Internal ID21946815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48896231..48896302hg38UCSC Ensembl
chr15:49188428..49188499hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605132
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037472
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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