A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550622



Internal ID20923761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30746264..30750183hg38UCSC Ensembl
chr1:31219111..31223030hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg383920
hg193920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252378
Samples
Known GenesLAPTM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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