A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690057



Internal ID18641652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:138599272..138630555hg38UCSC Ensembl
Innerchr8:139611515..139642798hg19UCSC Ensembl
Innerchr8:139680697..139711980hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3831284
hg1931284
hg1831284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033028
Supporting Variants
Samples
Known GenesCOL22A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690057
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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