A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610929



Internal ID16051652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33349274..33408762hg38UCSC Ensembl
Innerchr8:33206792..33266280hg19UCSC Ensembl
Innerchr8:33326334..33385822hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3859489
hg1959489
hg1859489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156593
SamplesHGDP00534
Known GenesFUT10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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