A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14036992



Internal ID21167290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32199930..32199930hg38UCSC Ensembl
chr14:32669136..32669136hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3064636
Supporting Variants
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)nssv14036992
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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