A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595116



Internal ID20968187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56459026..56459684hg38UCSC Ensembl
chr12:56852810..56853468hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595116
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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