A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563264



Internal ID20936335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56094443..56094886hg38UCSC Ensembl
chr8:57007002..57007445hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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