A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869525



Internal ID15816795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31262484..31266014hg38UCSC Ensembl
Innerchr17:29589502..29593032hg19UCSC Ensembl
Innerchr17:26613628..26617158hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383531
hg193531
hg183531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574670
Supporting Variants
Samples
Known GenesNF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869525
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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