A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171655



Internal ID22331402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118875315..118875618hg38UCSC Ensembl
chr1:119417938..119418241hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464925
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)nsv3171655
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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