A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14021229



Internal ID21171854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18174090..18174090hg38UCSC Ensembl
chr21:19546407..19546407hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3045005
Supporting Variants
SamplesNA12878
Known GenesCHODL
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)nssv14021229
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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