A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512577



Internal ID15852002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29825566..29829409hg38UCSC Ensembl
Outerchr19:30316473..30320316hg19UCSC Ensembl
Outerchr19:35008313..35012156hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg383844
hg193844
hg183844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625186
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)nsv512577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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