A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188160



Internal ID22340112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1012613..1018441hg38UCSC Ensembl
chr8:962613..968441hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg385829
hg195829
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8968n152
Supporting Variantsnssv14463942, nssv14462683
SamplesHG00733
Known GenesERICH1-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188160
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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