A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543442



Internal ID20916690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23332687..23334093hg38UCSC Ensembl
chr1:23659180..23660586hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250654
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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