A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548937



Internal ID20922115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51291559..51293367hg38UCSC Ensembl
chr1:51757231..51759039hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251651
Samples
Known GenesTTC39A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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