A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3045792



Internal ID21177838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29731575..29731575hg38UCSC Ensembl
chr4:29733197..29733197hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14030576
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)nsv3045792
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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