A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606984



Internal ID21799031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5928387..5931483hg38UCSC Ensembl
chr12:6037553..6040649hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383097
hg193097
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102118
Supporting Variants
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606984
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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