A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171888



Internal ID22331520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9129265..9129355hg38UCSC Ensembl
chr1:9189324..9189414hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv99n152
Supporting Variantsnssv14441199
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)nsv3171888
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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