A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560506



Internal ID20933577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80222131..80222626hg38UCSC Ensembl
chr5:79517950..79518445hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268961
Samples
Known GenesSERINC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560506
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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