A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589528



Internal ID20962599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30463292..30465406hg38UCSC Ensembl
chr12:30616225..30618339hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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