A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025858



Internal ID18768390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18177517..18279674hg38UCSC Ensembl
Innerchr8:18035026..18137183hg19UCSC Ensembl
Innerchr8:18079306..18181463hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38102158
hg19102158
hg18102158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3684191
Samples
Known GenesNAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025858
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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