A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539366



Internal ID20912664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113722576..113723480hg38UCSC Ensembl
chr1:114265198..114266102hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249221
Samples
Known GenesPHTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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