A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134959



Internal ID19275156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1207348..1207758hg38UCSC Ensembl
Outerchr1:1142728..1143138hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n106
Supporting Variantsnssv3988498
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134959
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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