A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512169



Internal ID15504908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495308..76501434hg38UCSC Ensembl
Outerchr10:78255066..78261192hg19UCSC Ensembl
Outerchr10:77925072..77931198hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386127
hg196127
hg186127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624734
Samples1
Known GenesC10orf11
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512169
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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