A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535617



Internal ID20908975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155797856..155798577hg38UCSC Ensembl
chr1:155767647..155768368hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247139
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535617
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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