A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581499



Internal ID20954570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55500737..55501335hg38UCSC Ensembl
chr15:55792935..55793533hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241070
Samples
Known GenesDYX1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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