A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891832



Internal ID15839102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566611..1567558hg38UCSC Ensembl
Innerchr19:1566610..1567557hg19UCSC Ensembl
Innerchr19:1517610..1518557hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38948
hg19948
hg18948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578308
Supporting Variants
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891832
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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