A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611086



Internal ID16051809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39551067..39665094hg38UCSC Ensembl
Innerchr8:39408586..39522613hg19UCSC Ensembl
Innerchr8:39527743..39641770hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38114028
hg19114028
hg18114028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1111256
Samples
Known GenesADAM18, LOC100130964
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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