A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177874



Internal ID22334672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2378444..2378508hg38UCSC Ensembl
chr7:2418079..2418143hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438237
SamplesHG00514
Known GenesEIF3B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177874
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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