A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607242



Internal ID16394651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62575192..63238576hg38UCSC Ensembl
Innerchr7:62035570..62698954hg19UCSC Ensembl
Innerchr7:61673005..62336389hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38663385
hg19663385
hg18663385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11396n54
Supporting Variantsnssv1085102
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607242
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