A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580798



Internal ID20953869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110008845..110009158hg38UCSC Ensembl
chr12:110446650..110446963hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221794
Samples
Known GenesANKRD13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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