A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562267



Internal ID16002990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71463462..71622849hg38UCSC Ensembl
Innerchr13:72037594..72196981hg19UCSC Ensembl
Innerchr13:70935595..71094982hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38159388
hg19159388
hg18159388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813823
Samples
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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