A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112153



Internal ID18940421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:2876495..2876642hg38UCSC Ensembl
Outerchr18:2876493..2876640hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965843
SamplesKWS1
Known GenesEMILIN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112153
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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