A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592913



Internal ID20965984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48570723..48571480hg38UCSC Ensembl
chr12:48964506..48965263hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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