A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150027



Internal ID15526625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6895855..7105125hg38UCSC Ensembl
Innerchr19:6895866..7105136hg19UCSC Ensembl
Innerchr19:6846866..7056136hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38209271
hg19209271
hg18209271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578466
Supporting Variants
SamplesHGDP00160
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)nssv1150027
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer