A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3045858



Internal ID21177904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143012549..143012549hg38UCSC Ensembl
chr5:142392114..142392114hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14022256
SamplesNA12878
Known GenesARHGAP26
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)nsv3045858
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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