A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172551



Internal ID22331864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139307958..139308008hg38UCSC Ensembl
chr6:139629095..139629145hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375592
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)nsv3172551
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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