A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577162



Internal ID20950233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112205153..112205768hg38UCSC Ensembl
chr12:112642957..112643572hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224325
Samples
Known GenesHECTD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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