A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036218



Internal ID21945561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50872626..50872711hg38UCSC Ensembl
chr12:51266409..51266494hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614481
Samples
Known GenesTMPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036218
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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