A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130308



Internal ID19274463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63931436..63934181hg38UCSC Ensembl
Outerchr11:63698908..63701653hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382746
hg192746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv664n106
Supporting Variantsnssv3966230, nssv3963536
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130308
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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