A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543770



Internal ID21868125
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 StatusS
Merged Variantsnsv5995685
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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