A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540307



Internal ID20913597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160177289..160178177hg38UCSC Ensembl
chr2:161033800..161034688hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n223
Supporting Variantsnssv18255383
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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