A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899978



Internal ID15847248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47687016..47689867hg38UCSC Ensembl
Innerchr19:48190273..48193124hg19UCSC Ensembl
Innerchr19:52882085..52884936hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382852
hg192852
hg182852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579892
Supporting Variants
Samples
Known GenesGLTSCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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