A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033208



Internal ID19122430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144992870..145072757hg38UCSC Ensembl
Innerchr8:146218256..146298143hg19UCSC Ensembl
Innerchr8:146189060..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3879888
hg1979888
hg1879888
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690898, nssv3690896, nssv3690906, nssv3690897, nssv3690902, nssv3690899, nssv3690904, nssv3690901, nssv3690900, nssv3690905, nssv3690903
Samples
Known GenesC8orf33, TMED10P1, ZNF252P, ZNF252P-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033208
Frequency
Sample Size11257
Observed Gain3
Observed Loss8
Observed Complex0
Frequencyn/a


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