A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3066486



Internal ID21197877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6036924..6036924hg38UCSC Ensembl
chr4:6038651..6038651hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14033544
SamplesCHM1
Known GenesJAKMIP1
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)nsv3066486
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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