A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589157



Internal ID20962228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75935346..75935701hg38UCSC Ensembl
chr12:76329126..76329481hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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