A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512162



Internal ID15504901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48707815..48711330hg38UCSC Ensembl
Outerchr10:49915860..49919375hg19UCSC Ensembl
Outerchr10:49585866..49589381hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383516
hg193516
hg183516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624726
Samples1
Known GenesWDFY4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512162
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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