A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611005



Internal ID16398414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39483411hg38UCSC Ensembl
Innerchr8:39237668..39340930hg19UCSC Ensembl
Innerchr8:39356825..39460087hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38103263
hg19103263
hg18103263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12096n54
Supporting Variantsnssv1110549, nssv1110538, nssv1110546, nssv1110545, nssv1110537, nssv1110547, nssv1110544, nssv1110543, nssv1110542, nssv1110539, nssv1110548, nssv1110541, nssv1110540
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611005
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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