A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562552



Internal ID16003275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83785734..83897817hg38UCSC Ensembl
Innerchr13:84359869..84471952hg19UCSC Ensembl
Innerchr13:83257870..83369953hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38112084
hg19112084
hg18112084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816603
Samples
Known GenesSLITRK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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