A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201365



Internal ID22350689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49302558..49302712hg38UCSC Ensembl
chr10:50510603..50510757hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438173
SamplesHG00514
Known GenesC10orf71
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201365
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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