A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147650



Internal ID19199763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93844826..93845046hg38UCSC Ensembl
Outerchr11:93577992..93578212hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996434
SamplesKWB1
Known GenesVSTM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147650
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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