A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200508



Internal ID22349661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5689769..5689944hg38UCSC Ensembl
chr10:5731732..5731907hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14415226
SamplesHG00514
Known GenesFAM208B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200508
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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