A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595292



Internal ID20968363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95053803..95055846hg38UCSC Ensembl
chr12:95447579..95449622hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382044
hg192044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1656n223
Supporting Variantsnssv18232302
Samples
Known GenesNR2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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