A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577822



Internal ID20950893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95044275..95044718hg38UCSC Ensembl
chr12:95438051..95438494hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231946
Samples
Known GenesNR2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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