A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432765



Internal ID22175614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9187907..9288394hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38100488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216144
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14432765
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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