A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594598



Internal ID20967669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96671136..96671674hg38UCSC Ensembl
chr12:97064914..97065452hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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