A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122581



Internal ID18931288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5637097..5637156hg38UCSC Ensembl
Outerchr11:5658327..5658386hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970792
SamplesKWS2
Known GenesTRIM34, TRIM6-TRIM34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122581
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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