A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134171



Internal ID18910647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102944730..102944787hg38UCSC Ensembl
Outerchr11:102815459..102815516hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971652
SamplesKWS2
Known GenesMMP13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134171
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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