A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553833



Internal ID20926946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28006117..28007342hg38UCSC Ensembl
chr1:28332628..28333853hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv139n223
Supporting Variantsnssv18249064
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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