A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555706



Internal ID20928777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22334776..22335594hg38UCSC Ensembl
chr8:22192289..22193107hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277468
Samples
Known GenesPIWIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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