A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562355



Internal ID16003078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635745..75636921hg38UCSC Ensembl
Innerchr13:76209881..76211057hg19UCSC Ensembl
Innerchr13:75107882..75109058hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381177
hg191177
hg181177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3258n54
Supporting Variantsnssv815776
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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