A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138641



Internal ID18906205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79751662..79751742hg38UCSC Ensembl
Outerchr18:77511662..77511742hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991224
SamplesKWS2
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138641
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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