A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578472



Internal ID16019195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6922724..7084736hg38UCSC Ensembl
Innerchr19:6922735..7084747hg19UCSC Ensembl
Innerchr19:6873735..7035747hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38162013
hg19162013
hg18162013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6237n54
Supporting Variantsnssv893196
Samples
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578472
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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