A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564115



Internal ID20937186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31849571..31850913hg38UCSC Ensembl
chr5:31849677..31851019hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268162
Samples
Known GenesPDZD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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