A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14420439



Internal ID22158048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29004116..29004601hg38UCSC Ensembl
chr19:29495023..29495508hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204268
Supporting Variants
SamplesHG00514
Known GenesLOC100505835
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14420439
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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