A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576546



Internal ID20949617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6706559..6707564hg38UCSC Ensembl
chr12:6815725..6816730hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1360n223
Supporting Variantsnssv18228281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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