A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277972



Internal ID20845012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39837558..39838517hg38UCSC Ensembl
chr8:39695077..39696036hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557979
Supporting Variants
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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