A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611581



Internal ID16398990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81130756..81134024hg38UCSC Ensembl
Innerchr8:82042991..82046259hg19UCSC Ensembl
Innerchr8:82205546..82208814hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383269
hg193269
hg183269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117023, nssv1117024
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611581
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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