A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554801



Internal ID15995524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55546675..55856884hg38UCSC Ensembl
Innerchr11:55314151..55624360hg19UCSC Ensembl
Innerchr11:55070727..55380936hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38310210
hg19310210
hg18310210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775161
Samples
Known GenesOR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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