A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059496



Internal ID19148715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21437988..21626623hg38UCSC Ensembl
Innerchr17:21341300..21529890hg19UCSC Ensembl
Innerchr17:21281893..21470483hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38188636
hg19188591
hg18188591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3124n100
Supporting Variantsnssv3720031
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)nsv1059496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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