A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542090



Internal ID20915356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164701696..165001499hg38UCSC Ensembl
chr1:164670933..164970736hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38299804
hg19299804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247993
Samples
Known GenesLOC100505795, PBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542090
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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