A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015577



Internal ID19104794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39373128..39527663hg38UCSC Ensembl
Innerchr8:39230647..39385182hg19UCSC Ensembl
Innerchr8:39349804..39504339hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38154536
hg19154536
hg18154536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3760585, nssv3684996, nssv3684998, nssv3684997, nssv3684999
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)nsv1015577
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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