A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578683



Internal ID16366092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14933745..14937733hg38UCSC Ensembl
Innerchr19:15044557..15048545hg19UCSC Ensembl
Innerchr19:14905557..14909545hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383989
hg193989
hg183989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6283n54
Supporting Variantsnssv894913
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578683
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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