A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411298



Internal ID22287152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152111644..152111747hg38UCSC Ensembl
chr4:153032796..153032899hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194427
Supporting Variants
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)nssv14411298
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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