A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512148



Internal ID15504887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13217002..13218889hg38UCSC Ensembl
Outerchr10:13259002..13260889hg19UCSC Ensembl
Outerchr10:13299008..13300895hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381888
hg191888
hg181888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624709
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)nsv512148
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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