A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578397



Internal ID16365806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2701508..2709347hg38UCSC Ensembl
Innerchr19:2701506..2709345hg19UCSC Ensembl
Innerchr19:2652506..2660345hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387840
hg197840
hg187840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6222n54
Supporting Variantsnssv892146
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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