A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14035899



Internal ID21166544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184235701..184235701hg38UCSC Ensembl
chr3:183953489..183953489hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3048838
Supporting Variants
SamplesNA12878
Known GenesVWA5B2
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)nssv14035899
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer