A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059795



Internal ID18802326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35828724..36157706hg38UCSC Ensembl
Innerchr17:34155728..34485079hg19UCSC Ensembl
Innerchr17:31179841..31509192hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38328983
hg19329352
hg18329352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561116, nssv3561117, nssv3720059, nssv3720058
Samples
Known GenesC17orf66, CCL14, CCL15, CCL15-CCL14, CCL16, CCL18, CCL23, CCL3, CCL4, CCL5, LYZL6, RDM1, TAF15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059795
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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