A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591673



Internal ID20964744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120188823..120189314hg38UCSC Ensembl
chr12:120626626..120627117hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219539
Samples
Known GenesGCN1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591673
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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