A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062622



Internal ID19151841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13352197..13473976hg38UCSC Ensembl
Innerchr17:13255514..13377293hg19UCSC Ensembl
Innerchr17:13196239..13318018hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38121780
hg19121780
hg18121780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560358
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062622
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer