A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556829



Internal ID20929900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42983176..42983616hg38UCSC Ensembl
chr8:42838319..42838759hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278074
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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