A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3064395



Internal ID21195886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86272070..86272070hg38UCSC Ensembl
chr11:85983112..85983112hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14016510
SamplesNA12878
Known GenesEED
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)nsv3064395
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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