A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611307



Internal ID16398716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48169149..48181329hg38UCSC Ensembl
Innerchr8:49081709..49093889hg19UCSC Ensembl
Innerchr8:49244262..49256442hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3812181
hg1912181
hg1812181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115106, nssv1115105
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611307
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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