A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556223



Internal ID20929294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73440764..73441637hg38UCSC Ensembl
chr7:72855094..72855967hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276483
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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