A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3049874



Internal ID21181923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60087706..60087843hg38UCSC Ensembl
chr20:58662761..58662898hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14025231
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)nsv3049874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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