A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129957



Internal ID19286338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:8934761..8934837hg38UCSC Ensembl
Outerchr18:8934759..8934835hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1544n106
Supporting Variantsnssv3965097
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129957
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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