A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110727



Internal ID18912381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14833877..14833969hg38UCSC Ensembl
Outerchr19:14944689..14944781hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961135
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110727
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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