A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059024



Internal ID19148243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21437988..21609743hg38UCSC Ensembl
Innerchr17:21341300..21513010hg19UCSC Ensembl
Innerchr17:21281893..21453603hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38171756
hg19171711
hg18171711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3124n100
Supporting Variantsnssv3560965
Samples
Known GenesC17orf51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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