A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028370



Internal ID19117588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:145021961..145072757hg38UCSC Ensembl
Innerchr8:146247347..146298143hg19UCSC Ensembl
Innerchr8:146218151..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3850797
hg1950797
hg1850797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7342n100
Supporting Variantsnssv3690914, nssv3690913, nssv3690918, nssv3758055, nssv3690915, nssv3690917, nssv3690919, nssv3690916
Samples
Known GenesC8orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028370
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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