A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027898



Internal ID18770429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39356415..39511377hg38UCSC Ensembl
Innerchr8:39213934..39368896hg19UCSC Ensembl
Innerchr8:39333091..39488053hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38154963
hg19154963
hg18154963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3685595
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)nsv1027898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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