A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546294



Internal ID20919512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47356268..47357902hg38UCSC Ensembl
chr1:47821940..47823574hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251161
Samples
Known GenesCMPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546294
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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