A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997621



Internal ID20564661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15501812..15502358hg38UCSC Ensembl
chr12:15654746..15655292hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470535
Supporting Variants
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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