A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561618



Internal ID16002341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49907577..51521449hg38UCSC Ensembl
Innerchr13:50481713..52095585hg19UCSC Ensembl
Innerchr13:49379714..50993586hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381613873
hg191613873
hg181613873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176446
SamplesHGDP00539
Known GenesDLEU1, DLEU2, DLEU7, DLEU7-AS1, FAM124A, GUCY1B2, INTS6, INTS6-AS1, KCNRG, LINC00371, MIR15A, MIR16-1, MIR3613, MIR5693, RNASEH2B, RNASEH2B-AS1, SERPINE3, SPRYD7, ST13P4, TRIM13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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