A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561830



Internal ID16349239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57982769..58025111hg38UCSC Ensembl
Innerchr13:58556903..58599245hg19UCSC Ensembl
Innerchr13:57454904..57497246hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3842343
hg1942343
hg1842343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812189
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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