A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14409161



Internal ID22327110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37036685..37036793hg38UCSC Ensembl
chr4:37038307..37038415hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3281824
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14409161
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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