A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390468



Internal ID22304832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9123310..9123394hg38UCSC Ensembl
chr1:9183369..9183453hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204732
Supporting Variants
SamplesNA19240
Known GenesGPR157
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390468
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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