A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031982



Internal ID18774516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:47085392..47198972hg38UCSC Ensembl
Innerchr8:47997015..48110595hg19UCSC Ensembl
Innerchr8:48116180..48229760hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38113581
hg19113581
hg18113581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687458
Samples
Known GenesLOC100287846
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031982
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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