A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569763



Internal ID20942834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168569289..168570202hg38UCSC Ensembl
chr5:167996294..167997207hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6023n223
Supporting Variantsnssv18267599
Samples
Known GenesPANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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