A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144863



Internal ID18925364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9900824..9901424hg38UCSC Ensembl
Outerchr19:10011500..10012100hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1710n106
Supporting Variantsnssv3981462
SamplesKWS1
Known GenesOLFM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144863
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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