A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110494



Internal ID18918086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12131039..12131318hg38UCSC Ensembl
Outerchr11:12152586..12152865hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv588n106
Supporting Variantsnssv3960145
SamplesKWS1
Known GenesMICAL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110494
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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