A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586653



Internal ID20959724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71687401..71688236hg38UCSC Ensembl
chr12:72081181..72082016hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232808
Samples
Known GenesTMEM19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586653
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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