A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118786



Internal ID19254957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:34493636..34493936hg38UCSC Ensembl
Outerchr18:32073600..32073900hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981098
SamplesKWS1
Known GenesDTNA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118786
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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