A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574714



Internal ID16015437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33640441..34608994hg38UCSC Ensembl
Innerchr17:31967460..32936013hg19UCSC Ensembl
Innerchr17:28991573..29960126hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38968554
hg19968554
hg18968554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869638
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574714
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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