A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578688



Internal ID16366097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14934418..14937833hg38UCSC Ensembl
Innerchr19:15045230..15048645hg19UCSC Ensembl
Innerchr19:14906230..14909645hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383416
hg193416
hg183416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6283n54
Supporting Variantsnssv894936, nssv894938, nssv894937, nssv894935
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578688
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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