A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593175



Internal ID20966246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109954795..109955257hg38UCSC Ensembl
chr12:110392600..110393062hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228537
Samples
Known GenesGIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593175
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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