A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552579



Internal ID20925704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44685520..44686629hg38UCSC Ensembl
chr1:45151192..45152301hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251848
Samples
Known GenesC1orf228
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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