A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174403



Internal ID22332793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232456744..232457159hg38UCSC Ensembl
chr2:233321454..233321869hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14406573
SamplesNA19240
Known GenesALPI
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174403
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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