A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14037375



Internal ID21167547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23790312..23790312hg38UCSC Ensembl
chr10:24079241..24079241hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3064227
Supporting Variants
SamplesNA12878
Known GenesKIAA1217
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)nssv14037375
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