A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548272



Internal ID20921464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89656954..89658524hg38UCSC Ensembl
chr1:90122513..90124083hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251970
Samples
Known GenesLRRC8C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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