A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145538



Internal ID19272417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63319320..63319374hg38UCSC Ensembl
Outerchr11:63086792..63086846hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983178
SamplesKWS1
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145538
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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