A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14035905



Internal ID21158134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59282717..59282717hg38UCSC Ensembl
chr11:59050190..59050190hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3065866
Supporting Variants
SamplesCHM1
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)nssv14035905
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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