A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550023



Internal ID20923175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77661225..77662180hg38UCSC Ensembl
chr1:78126910..78127865hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253158
Samples
Known GenesZZZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550023
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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