A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733930



Internal ID20509862
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 StatusM
Merged Variants
Supporting Variantsnssv16289367
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733930
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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