A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684212



Internal ID18635807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994017..19008815hg38UCSC Ensembl
Innerchr8:18851527..18866325hg19UCSC Ensembl
Innerchr8:18895807..18910605hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814799
hg1914799
hg1814799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023757
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3684212
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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