A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109550



Internal ID18940554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136760107..136760159hg38UCSC Ensembl
Outerchr3:136478949..136479001hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957045
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109550
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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