A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133820



Internal ID18910002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:18354841..18354891hg38UCSC Ensembl
Outerchr1:18681335..18681385hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970144
SamplesKWS2
Known GenesIGSF21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133820
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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