A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019412



Internal ID19108630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16093369..16163959hg38UCSC Ensembl
Innerchr8:15950878..16021468hg19UCSC Ensembl
Innerchr8:15995249..16065839hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3870591
hg1970591
hg1870591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7109n100
Supporting Variantsnssv3760244
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)nsv1019412
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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