A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3056359



Internal ID21188261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199777..31199777hg38UCSC Ensembl
chr19:31690683..31690683hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14022695
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)nsv3056359
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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