A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062220



Internal ID18804751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15966243..16189842hg38UCSC Ensembl
Innerchr17:15869557..16093156hg19UCSC Ensembl
Innerchr17:15810282..16033881hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38223600
hg19223600
hg18223600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3108n100
Supporting Variantsnssv3719934
Samples
Known GenesADORA2B, NCOR1, TTC19, ZSWIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062220
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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