A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277889



Internal ID20844929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37986988..37988069hg38UCSC Ensembl
chr8:37844506..37845587hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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