A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610319



Internal ID16397728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12141163..12176432hg38UCSC Ensembl
Innerchr8:11998672..12033941hg19UCSC Ensembl
Innerchr8:12036081..12071350hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3835270
hg1935270
hg1835270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106605
Samples
Known GenesFAM66D, FAM90A2P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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