A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128820



Internal ID19273792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:44183935..44197335hg38UCSC Ensembl
Outerchr18:41763900..41777300hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1589n106
Supporting Variantsnssv3961488
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128820
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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