A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611057



Internal ID16398466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39451651..39499982hg38UCSC Ensembl
Innerchr8:39309170..39357501hg19UCSC Ensembl
Innerchr8:39428327..39476658hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3848332
hg1948332
hg1848332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12107n54
Supporting Variantsnssv1111214, nssv1111213
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611057
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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