A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580107



Internal ID16020830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53574616..53713042hg38UCSC Ensembl
Innerchr19:54077870..54216296hg19UCSC Ensembl
Innerchr19:58769682..58908108hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38138427
hg19138427
hg18138427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901187
Samples
Known GenesDPRX, LOC284379, MIR1283-1, MIR1323, MIR498, MIR512-1, MIR512-2, MIR515-1, MIR515-2, MIR517A, MIR518B, MIR518C, MIR518F, MIR519B, MIR519C, MIR519E, MIR520A, MIR520B, MIR520C, MIR520E, MIR520F, MIR523, MIR524, MIR525, MIR526A1, MIR526B, ZNF331
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580107
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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