A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199013



Internal ID22348661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154202312..154286912hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3884601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14413756
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)nsv3199013
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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