A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026877



Internal ID19116095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:41184230..41218221hg38UCSC Ensembl
Innerchr8:41041749..41075740hg19UCSC Ensembl
Innerchr8:41160906..41194897hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3833992
hg1933992
hg1833992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757233
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)nsv1026877
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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