A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv535282



Internal ID15158920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6895855..7105125hg38UCSC Ensembl
Innerchr19:6895866..7105136hg19UCSC Ensembl
Innerchr19:6846866..7056136hg18UCSC Ensembl
Innerchr19:6846866..7056136hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38209271
hg19209271
hg18209271
hg17209271
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv458337
Supporting Variants
SamplesHGDP00160
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nssv535282
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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