A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015809



Internal ID19105027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:41375834..41414845hg38UCSC Ensembl
Innerchr8:41233353..41272364hg19UCSC Ensembl
Innerchr8:41352510..41391521hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3839012
hg1939012
hg1839012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757234
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)nsv1015809
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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