A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144576



Internal ID19255070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72850549..72850605hg38UCSC Ensembl
Outerchr11:72561594..72561650hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995416
SamplesKWS1
Known GenesFCHSD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144576
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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