A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200382



Internal ID22349841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23187120..23187196hg38UCSC Ensembl
chr10:23476049..23476125hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438291
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)nsv3200382
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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