A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535849



Internal ID20909203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161263875..161264543hg38UCSC Ensembl
chr1:161233665..161234333hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247345
Samples
Known GenesPCP4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535849
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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