A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183628



Internal ID22337723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159205706..159206032hg38UCSC Ensembl
chr1:159175496..159175822hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455452
SamplesHG00733
Known GenesDARC
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183628
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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