A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585425



Internal ID20958496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1440406..2565306hg38UCSC Ensembl
chr12:1549572..2674472hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381124901
hg191124901
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222240
Samples
Known GenesADIPOR2, CACNA1C, CACNA1C-AS4, CACNA1C-IT3, CACNA2D4, DCP1B, ERC1, FBXL14, LINC00940, LINC00942, LRTM2, MIR3649, WNT5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585425
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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