A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606607



Internal ID16394016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:33092117..33152890hg38UCSC Ensembl
Innerchr7:33131729..33192502hg19UCSC Ensembl
Innerchr7:33098254..33159027hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3860774
hg1960774
hg1860774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11272n54
Supporting Variantsnssv1082694
Samples
Known GenesBBS9, RP9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606607
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