A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594677



Internal ID20967748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4324943..4325576hg38UCSC Ensembl
chr12:4434109..4434742hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225698
Samples
Known GenesC12orf5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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