A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591263



Internal ID20964334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56415830..56417034hg38UCSC Ensembl
chr12:56809614..56810818hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224079
Samples
Known GenesTIMELESS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591263
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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