A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559925



Internal ID20932996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137920732..137923184hg38UCSC Ensembl
chr5:137256421..137258873hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg382453
hg192453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266786
Samples
Known GenesPKD2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559925
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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