A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551616



Internal ID20924747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95139025..95139561hg38UCSC Ensembl
chr1:95604581..95605117hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253965
Samples
Known GenesTMEM56, TMEM56-RWDD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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