A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545378



Internal ID20918609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56664273..56664397hg38UCSC Ensembl
chr1:57129946..57130070hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249837
Samples
Known GenesPRKAA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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