A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611003



Internal ID16398412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39473491hg38UCSC Ensembl
Innerchr8:39237668..39331010hg19UCSC Ensembl
Innerchr8:39356825..39450167hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3893343
hg1993343
hg1893343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12096n54
Supporting Variantsnssv1110514, nssv1110513, nssv1110512, nssv1110515
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611003
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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