A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170440



Internal ID22330750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15485508..15485591hg38UCSC Ensembl
chr2:15625632..15625715hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14393586
SamplesNA19240
Known GenesNBAS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170440
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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