A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278048



Internal ID20845088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42528172..42528969hg38UCSC Ensembl
chr8:42383312..42384112hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38798
hg19801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565405
Supporting Variants
Samples
Known GenesSLC20A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278048
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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