A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174803



Internal ID15534350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61492279..61603811hg38UCSC Ensembl
Innerchr11:61259751..61371283hg19UCSC Ensembl
Innerchr11:61016327..61127859hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38111533
hg19111533
hg18111533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555169
Supporting Variants
SamplesNINDS_61
Known GenesLRRC10B, MIR4488, SYT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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