A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624723



Internal ID15848259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32414966..32418224hg38UCSC Ensembl
Outerchr10:32703894..32707152hg19UCSC Ensembl
Outerchr10:32743900..32747158hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383259
hg193259
hg183259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512159
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624723
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer