A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14029979



Internal ID21159253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199765..31199765hg38UCSC Ensembl
chr19:31690671..31690671hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3058216
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)nssv14029979
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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