A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397871



Internal ID22327906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26181042..26181042hg38UCSC Ensembl
chr4:26182664..26182664hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383825
hg193825
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3541008
Supporting Variants
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)nssv14397871
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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