A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027325



Internal ID19116544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9406895..9475697hg38UCSC Ensembl
Innerchr8:9264405..9333207hg19UCSC Ensembl
Innerchr8:9301815..9370617hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3868803
hg1968803
hg1868803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681706
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)nsv1027325
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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