A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611002



Internal ID16398411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39472638hg38UCSC Ensembl
Innerchr8:39237668..39330157hg19UCSC Ensembl
Innerchr8:39356825..39449314hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3892490
hg1992490
hg1892490
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12102n54
Supporting Variantsnssv1110509, nssv1110510, nssv1110511
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611002
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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