A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277733



Internal ID20844773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31008424..31009163hg38UCSC Ensembl
chr8:30865940..30866679hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570228
Supporting Variants
Samples
Known GenesPURG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277733
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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