A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175601



Internal ID22333447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6022311..6022429hg38UCSC Ensembl
chr2:6162443..6162561hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392899
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)nsv3175601
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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