A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565672



Internal ID20938743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168569414..168570144hg38UCSC Ensembl
chr5:167996419..167997149hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6023n223
Supporting Variantsnssv18267600
Samples
Known GenesPANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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