A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554662



Internal ID20927756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63632869..63633774hg38UCSC Ensembl
chr1:64098540..64099445hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv215n223
Supporting Variantsnssv18250605
Samples
Known GenesPGM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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