A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138205



Internal ID19286677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:27043423..27043477hg38UCSC Ensembl
Outerchr13:27617560..27617614hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990757
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138205
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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