A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120602



Internal ID19263090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63931422..63934178hg38UCSC Ensembl
Outerchr11:63698894..63701650hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv664n106
Supporting Variantsnssv3963015
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120602
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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