A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552717



Internal ID20925843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6551661..6552382hg38UCSC Ensembl
chr1:6611721..6612442hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251239
Samples
Known GenesNOL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552717
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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