A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178078



Internal ID22334790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149994895..149994995hg38UCSC Ensembl
chr4:150916047..150916147hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14425437
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178078
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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