A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556896



Internal ID20929967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118694933..118695292hg38UCSC Ensembl
chr4:119616088..119616447hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264185
Samples
Known GenesMETTL14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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