A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197460



Internal ID21336256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55512478..55512548hg38UCSC Ensembl
chr5:54808306..54808376hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927591
Supporting Variants
SamplesHG002
Known GenesPPAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197460
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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