A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553342



Internal ID20926450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37502760..37503570hg38UCSC Ensembl
chr1:37968361..37969171hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251072
Samples
Known GenesMEAF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553342
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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