A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289367



Internal ID20498585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15513072..15513146hg38UCSC Ensembl
chr12:15666006..15666080hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733930
Supporting Variants
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289367
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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