A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455452



Internal ID22249869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159205706..159206032hg38UCSC Ensembl
chr1:159175496..159175822hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183628
Supporting Variants
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)nssv14455452
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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