A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3046773



Internal ID21178819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173735918..173735918hg38UCSC Ensembl
chr5:173162921..173162921hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14029310
SamplesNA12878
Known GenesLOC101928136
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)nsv3046773
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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