A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556172



Internal ID20929243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35046361..35047147hg38UCSC Ensembl
chr8:34903879..34904665hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556172
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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