A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189187



Internal ID22340644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71238296..71238474hg38UCSC Ensembl
chr1:71703979..71704157hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14374798
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)nsv3189187
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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