A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602334



Internal ID21794381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71665894..71666281hg38UCSC Ensembl
chr12:72059674..72060061hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039213
Supporting Variants
Samples
Known GenesTHAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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