A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578687



Internal ID16366096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14934418..14937733hg38UCSC Ensembl
Innerchr19:15045230..15048545hg19UCSC Ensembl
Innerchr19:14906230..14909545hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383316
hg193316
hg183316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6283n54
Supporting Variantsnssv894932, nssv894933, nssv894934
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578687
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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