A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602736



Internal ID21794783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9062092..9062151hg38UCSC Ensembl
chr12:9214688..9214747hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037523
Supporting Variants
Samples
Known GenesLINC00612
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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