A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608958



Internal ID16396367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147582855..147585235hg38UCSC Ensembl
Innerchr7:147279947..147282327hg19UCSC Ensembl
Innerchr7:146910880..146913260hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382381
hg192381
hg182381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11707n54
Supporting Variantsnssv1098078
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608958
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