A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588517



Internal ID20961588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101912886..101913701hg38UCSC Ensembl
chr12:102306664..102307479hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1674n223
Supporting Variantsnssv18233604
Samples
Known GenesDRAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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