A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541097



Internal ID20914383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21738374..21739381hg38UCSC Ensembl
chr1:22064867..22065874hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248608
Samples
Known GenesUSP48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541097
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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