A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143685



Internal ID19277233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64035528..64036328hg38UCSC Ensembl
Outerchr11:63803000..63803800hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994374
SamplesKWS1
Known GenesMACROD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143685
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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