A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519297



Internal ID15099904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33640660..34608994hg38UCSC Ensembl
Innerchr17:31967679..32936013hg19UCSC Ensembl
Innerchr17:28991792..29960126hg18UCSC Ensembl
Innerchr17:28991792..29960126hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38968335
hg19968335
hg18968335
hg17968335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696774
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519297
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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