A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547629



Internal ID21871984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15470667..15470723hg38UCSC Ensembl
chr4:15472291..15472347hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995668
Supporting Variants
Samples
Known GenesCC2D2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547629
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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