A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511683



Internal ID15851108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23992379..23995701hg38UCSC Ensembl
Outerchr1:24318869..24322191hg19UCSC Ensembl
Outerchr1:24191456..24194778hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383323
hg193323
hg183323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626322
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)nsv511683
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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