A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587906



Internal ID20960977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100552794..100553144hg38UCSC Ensembl
chr12:100946572..100946922hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221437
Samples
Known GenesNR1H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587906
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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