A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3062631



Internal ID21194164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48964926..48964926hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14015887
SamplesCHM1
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)nsv3062631
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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