A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556755



Internal ID20929826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55897307..55898091hg38UCSC Ensembl
chr4:56763473..56764257hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266433
Samples
Known GenesEXOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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