A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760469



Internal ID18712064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18325949..18402503hg38UCSC Ensembl
Innerchr8:18183458..18260013hg19UCSC Ensembl
Innerchr8:18227738..18304293hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3876555
hg1976556
hg1876556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017393
Supporting Variants
Samples
Known GenesNAT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760469
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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