A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512130



Internal ID15851555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137564851..137568246hg38UCSC Ensembl
Outerchr9:140459303..140462698hg19UCSC Ensembl
Outerchr9:139579124..139582519hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383396
hg193396
hg183396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624690
Samples1
Known GenesDPH7
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512130
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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