A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612276



Internal ID21804323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3810697..3810787hg38UCSC Ensembl
chr12:3919863..3919953hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022573
Supporting Variants
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612276
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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