A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564145



Internal ID20937216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138390110..138391003hg38UCSC Ensembl
chr4:139311264..139312157hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5472n223
Supporting Variantsnssv18263157
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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