A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3065826



Internal ID21197256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101925713..101925713hg38UCSC Ensembl
chr11:101796444..101796444hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14034546
SamplesCHM1
Known GenesKIAA1377
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)nsv3065826
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