A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893195



Internal ID15840465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6916482..7105125hg38UCSC Ensembl
Innerchr19:6916493..7105136hg19UCSC Ensembl
Innerchr19:6867493..7056136hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38188644
hg19188644
hg18188644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578470
Supporting Variants
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)nssv893195
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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