A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582908



Internal ID20955979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21009536..21010696hg38UCSC Ensembl
chr12:21162470..21163630hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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