A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611609



Internal ID16399018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81763310..81844856hg38UCSC Ensembl
Innerchr8:82675545..82757091hg19UCSC Ensembl
Innerchr8:82838100..82919646hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3881547
hg1981547
hg1881547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156618
SamplesHGDP01077
Known GenesSNX16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611609
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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