A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576350



Internal ID20949421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57900399..57900890hg38UCSC Ensembl
chr12:58294182..58294673hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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