A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592407



Internal ID20965478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100074402..100075288hg38UCSC Ensembl
chr12:100468180..100469066hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223117
Samples
Known GenesUHRF1BP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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