A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707005



Internal ID21379281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59131752..59132017hg38UCSC Ensembl
chr1:59597424..59597689hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391012
Supporting Variants
Samples
Known GenesHSD52
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707005
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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