A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3541008



Internal ID22410126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26181042..26181042hg38UCSC Ensembl
chr4:26182664..26182664hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381839
hg191839
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14397871, nssv14424226
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3541008
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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