A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606711



Internal ID16047434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40185530..40320658hg38UCSC Ensembl
Innerchr7:40225129..40360257hg19UCSC Ensembl
Innerchr7:40191654..40326782hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38135129
hg19135129
hg18135129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11290n54
Supporting Variantsnssv1083047
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606711
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