A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561481



Internal ID16002204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34989723..34996546hg38UCSC Ensembl
Innerchr13:35563860..35570683hg19UCSC Ensembl
Innerchr13:34461860..34468683hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386824
hg196824
hg186824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807720
Samples
Known GenesNBEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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