A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122609



Internal ID19272948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:42821791..42821844hg38UCSC Ensembl
Outerchr11:42843341..42843394hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970458, nssv3995386
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122609
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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