A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194444



Internal ID22344756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35105932..35106129hg38UCSC Ensembl
chr19:35596836..35597033hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420481
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)nsv3194444
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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