A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558011



Internal ID20931082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64872794..64873165hg38UCSC Ensembl
chr4:65738512..65738883hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5300n223
Supporting Variantsnssv18266522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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