A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578338



Internal ID16019061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1847699..1869095hg38UCSC Ensembl
Innerchr19:1847698..1869094hg19UCSC Ensembl
Innerchr19:1798698..1820094hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3821397
hg1921397
hg1821397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891944
Samples
Known GenesKLF16, REXO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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