A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057286



Internal ID18799817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6957866..7048627hg38UCSC Ensembl
Innerchr19:6957877..7048638hg19UCSC Ensembl
Innerchr19:6908877..6999638hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3890762
hg1990762
hg1890762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564661
Samples
Known GenesEMR4P, FLJ25758, MBD3L4, MBD3L5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057286
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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