A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3538996



Internal ID22408167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1572204..1572204hg38UCSC Ensembl
chr2:1575976..1575976hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392871
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)nsv3538996
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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