A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14409164



Internal ID22317989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37460968..37462157hg38UCSC Ensembl
chr4:37462590..37463779hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186563
Supporting Variants
SamplesNA19240
Known GenesC4orf19
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14409164
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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