A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587156



Internal ID20960227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1094261..1095230hg38UCSC Ensembl
chr12:1203427..1204396hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38970
hg19970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220793
Samples
Known GenesERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587156
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer