A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121479



Internal ID18912911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106710218..106710330hg38UCSC Ensembl
Outerchr11:106580944..106581056hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965480
SamplesKWS2
Known GenesGUCY1A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121479
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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