A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579357



Internal ID20952428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53608097..53609338hg38UCSC Ensembl
chr12:54001881..54003122hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229044
Samples
Known GenesATF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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