A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574707



Internal ID20947778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87857761..87858921hg38UCSC Ensembl
chr8:88869989..88871149hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7413n223
Supporting Variantsnssv18278967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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