A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3058812



Internal ID21190574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708224..165708224hg38UCSC Ensembl
chr1:165677461..165677461hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14021987
SamplesCHM1
Known GenesLOC440700
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)nsv3058812
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