A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555329



Internal ID20928421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52083779..52084287hg38UCSC Ensembl
chr1:52549451..52549959hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249691
Samples
Known GenesBTF3L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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