A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567028



Internal ID20940099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41538860..41539181hg38UCSC Ensembl
chr8:41396379..41396700hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278013
Samples
Known GenesGINS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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