A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557078



Internal ID20930149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80506361..80507305hg38UCSC Ensembl
chr8:81418596..81419540hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278811
Samples
Known GenesZBTB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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