A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150653



Internal ID15875873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48680448..48699602hg38UCSC Ensembl
Innerchr19:49183705..49202859hg19UCSC Ensembl
Innerchr19:53875517..53894671hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3819155
hg1919155
hg1819155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579904
Supporting Variants
SamplesHGDP00748
Known GenesFUT2, SEC1P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150653
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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