A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277711



Internal ID20844751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30695427..30695760hg38UCSC Ensembl
chr8:30552944..30553277hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557311
Supporting Variants
Samples
Known GenesGSR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277711
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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