A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026186



Internal ID18768718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18325949..18403505hg38UCSC Ensembl
Innerchr8:18183458..18261015hg19UCSC Ensembl
Innerchr8:18227738..18305295hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3877557
hg1977558
hg1877558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7125n100
Supporting Variantsnssv3760470
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)nsv1026186
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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