A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588424



Internal ID20961495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95459240..95460004hg38UCSC Ensembl
chr12:95853016..95853780hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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