A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578631



Internal ID20951702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101398113..101398741hg38UCSC Ensembl
chr12:101791891..101792519hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227586
Samples
Known GenesARL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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