A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015198



Internal ID19104415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114589534..114629490hg38UCSC Ensembl
Innerchr8:115601763..115641719hg19UCSC Ensembl
Innerchr8:115670939..115710895hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3839957
hg1939957
hg1839957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7293n100
Supporting Variantsnssv3691330
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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