A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018828



Internal ID18761361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8752370..8933150hg38UCSC Ensembl
Innerchr8:8609880..8790660hg19UCSC Ensembl
Innerchr8:8647290..8828070hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38180781
hg19180781
hg18180781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681689
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018828
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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