A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122809



Internal ID19286468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39958769..39958820hg38UCSC Ensembl
Outerchr13:40532906..40532957hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971401, nssv3983041
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122809
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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