A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3754234



Internal ID18705829
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 StatusS
Merged Variantsnsv1032725
Supporting Variants
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)nssv3754234
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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