A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032725



Internal ID18775259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10704452..10728173hg38UCSC Ensembl
Innerchr8:10561962..10585683hg19UCSC Ensembl
Innerchr8:10599372..10623093hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3823722
hg1923722
hg1823722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3754234
Samples
Known GenesSOX7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032725
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer