A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575324



Internal ID20948395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156837631..156837690hg38UCSC Ensembl
chr5:156264642..156264701hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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