A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578465



Internal ID16019188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6895855..7103531hg38UCSC Ensembl
Innerchr19:6895866..7103542hg19UCSC Ensembl
Innerchr19:6846866..7054542hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38207677
hg19207677
hg18207677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6237n54
Supporting Variantsnssv893190, nssv893189
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)nsv578465
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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