A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561134



Internal ID20934205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27855404..28028320hg38UCSC Ensembl
chr5:27855511..28028427hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38172917
hg19172917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561134
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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