A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3063301



Internal ID21194831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117910277..117910552hg38UCSC Ensembl
chr3:117629124..117629399hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14034459
SamplesNA12878
Known Genes
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)nsv3063301
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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