A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578166



Internal ID16365575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:746206..753990hg38UCSC Ensembl
Innerchr19:746206..753990hg19UCSC Ensembl
Innerchr19:697206..704990hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387785
hg197785
hg187785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891235
Samples
Known GenesMISP, PALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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