A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181635



Internal ID22336676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60586436..60586530hg38UCSC Ensembl
chr1:61052108..61052202hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438844
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)nsv3181635
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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