A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563555



Internal ID20936626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61693566..61693813hg38UCSC Ensembl
chr8:62606125..62606372hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278397
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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