A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030811



Internal ID19120030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131703916..131720073hg38UCSC Ensembl
Innerchr8:132716163..132732320hg19UCSC Ensembl
Innerchr8:132785345..132801502hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3816158
hg1916158
hg1816158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691536
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)nsv1030811
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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