A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118360



Internal ID18906620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:16676152..16676299hg38UCSC Ensembl
Outerchr19:16786963..16787110hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981041
SamplesKWS1
Known GenesTMEM38A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118360
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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