A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702819



Internal ID126485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53540874..53685000hg38UCSC Ensembl
chr15:53833071..53977197hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38144127
hg19144127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522756
Supporting Variants
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702819
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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