A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134692



Internal ID18924385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:4324711..4324782hg38UCSC Ensembl
Outerchr18:4324711..4324782hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1538n106
Supporting Variantsnssv3972568
SamplesKWS2
Known GenesDLGAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134692
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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