A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609118



Internal ID16396527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155142791..155163953hg38UCSC Ensembl
Innerchr7:154934501..154955663hg19UCSC Ensembl
Innerchr7:154565434..154586596hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3821163
hg1921163
hg1821163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100257
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609118
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