A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3044896



Internal ID21176532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009496..11009496hg38UCSC Ensembl
chr20:10990144..10990144hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14032532
SamplesNA12878
Known Genes
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nsv3044896
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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