A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583760



Internal ID20956831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101758302..101759122hg38UCSC Ensembl
chr12:102152080..102152900hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1673n223
Supporting Variantsnssv18224235
Samples
Known GenesGNPTAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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