A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180075



Internal ID22335895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9129267..9129358hg38UCSC Ensembl
chr1:9189326..9189417hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv99n152
Supporting Variantsnssv14412701
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)nsv3180075
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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