A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148645



Internal ID18848703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14852271..14903451hg38UCSC Ensembl
Outerchr19:14963083..15014263hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851181
hg1951181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000681
SamplesKWB1
Known GenesOR7A17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148645
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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