A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995685



Internal ID21905028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791537..15791635hg38UCSC Ensembl
chr4:15793160..15793258hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543770
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995685
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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