A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587301



Internal ID20960372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64185270..64186200hg38UCSC Ensembl
chr12:64579050..64579980hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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