A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016636



Internal ID19105853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092468..16167255hg38UCSC Ensembl
Innerchr8:15949977..16024764hg19UCSC Ensembl
Innerchr8:15994348..16069135hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3874788
hg1974788
hg1874788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7109n100
Supporting Variantsnssv3675951
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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