A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605696



Internal ID16046419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:873118..980636hg38UCSC Ensembl
Innerchr7:912755..1020272hg19UCSC Ensembl
Innerchr7:879281..986798hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38107519
hg19107518
hg18107518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11111n54
Supporting Variantsnssv1077806
Samples
Known GenesADAP1, COX19, GET4, SUN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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