A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544964



Internal ID20918202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47335481..47335806hg38UCSC Ensembl
chr1:47801153..47801478hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251160
Samples
Known GenesCMPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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