A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017740



Internal ID18760274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39654455..39728857hg38UCSC Ensembl
Innerchr8:39511974..39586376hg19UCSC Ensembl
Innerchr8:39631131..39705533hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3874403
hg1974403
hg1874403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687208
Samples
Known GenesADAM18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017740
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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