A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512155



Internal ID15504894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29422644..29424461hg38UCSC Ensembl
Outerchr10:29711573..29713390hg19UCSC Ensembl
Outerchr10:29751579..29753396hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381818
hg191818
hg181818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624718
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)nsv512155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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