A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3066598



Internal ID21197975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44296935..44296935hg38UCSC Ensembl
chr6:44264672..44264672hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14038106
SamplesCHM1
Known GenesTCTE1
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)nsv3066598
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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