A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594538



Internal ID20967609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12336624..12337162hg38UCSC Ensembl
chr12:12489558..12490096hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227618
Samples
Known GenesMANSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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