A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064959



Internal ID19154178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41266750..41291759hg38UCSC Ensembl
Innerchr17:39423002..39448011hg19UCSC Ensembl
Innerchr17:36676528..36701537hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3825010
hg1925010
hg1825010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3170n100
Supporting Variantsnssv3544174
Samples
Known GenesKRTAP9-7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064959
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