A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562358



Internal ID16003081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635949..75636606hg38UCSC Ensembl
Innerchr13:76210085..76210742hg19UCSC Ensembl
Innerchr13:75108086..75108743hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38658
hg19658
hg18658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3259n54
Supporting Variantsnssv815779
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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