A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177626



Internal ID22334528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59946267..59946431hg38UCSC Ensembl
chr1:60411939..60412103hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14413159
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)nsv3177626
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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