A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579347



Internal ID20952418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122874653..122875356hg38UCSC Ensembl
chr12:123359200..123359903hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235317
Samples
Known GenesVPS37B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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