A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026873



Internal ID18769404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39345917..39529434hg38UCSC Ensembl
Innerchr8:39203436..39386953hg19UCSC Ensembl
Innerchr8:39322593..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38183518
hg19183518
hg18183518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3685592
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026873
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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