A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118216



Internal ID19266359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67289029..67289629hg38UCSC Ensembl
Outerchr11:67056500..67057100hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980885
SamplesKWS1
Known GenesANKRD13D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118216
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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