A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170632



Internal ID22330855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986781..32988365hg38UCSC Ensembl
chr1:33452382..33453966hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n152
Supporting Variantsnssv14413555
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170632
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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