A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442010



Internal ID22238320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52643568..52643568hg38UCSC Ensembl
chr10:54403328..54403328hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3544375
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14442010
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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