A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202236



Internal ID22351425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42251315..42262317hg38UCSC Ensembl
chr4:42253332..42264334hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3811003
hg1911003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6564n152
Supporting Variantsnssv14409178
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202236
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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