A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14420481



Internal ID22158116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35105932..35106129hg38UCSC Ensembl
chr19:35596836..35597033hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194444
Supporting Variants
SamplesHG00514
Known GenesHPN-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14420481
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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