A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110307



Internal ID19283266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:15326101..15331301hg38UCSC Ensembl
Outerchr18:15326100..15331300hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959953
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110307
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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