A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127216



Internal ID19265388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:86308269..86308373hg38UCSC Ensembl
Outerchr11:86019311..86019415hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985599
SamplesKWS1
Known GenesC11orf73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127216
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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