A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14433908



Internal ID22176871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202203775..202206437hg38UCSC Ensembl
chr1:202172903..202175565hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186264
Supporting Variants
SamplesHG00514
Known GenesLGR6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14433908
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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