A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3058979



Internal ID21190738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14833946..14833946hg38UCSC Ensembl
chr4:14835570..14835570hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14019902
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)nsv3058979
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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