A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172990



Internal ID22332092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110310153..110310232hg38UCSC Ensembl
chr1:110852775..110852854hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv371n152
Supporting Variantsnssv14413638
SamplesHG00514
Known GenesLOC440600
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3172990
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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