A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556523



Internal ID20929594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31002550..31003643hg38UCSC Ensembl
chr8:30860066..30861159hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277731
Samples
Known GenesPURG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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