A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584390



Internal ID20957461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43796697..43800288hg38UCSC Ensembl
chr12:44190500..44194091hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383592
hg193592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233113
Samples
Known GenesTWF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584390
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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