A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171021



Internal ID22331056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8610693..8611104hg38UCSC Ensembl
chr2:8750823..8751234hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14448879
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171021
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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