A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2829249



Internal ID15377635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36211245..36212891hg38UCSC Ensembl
Innerchr17:34538647..34540293hg19UCSC Ensembl
Innerchr17:31562760..31564406hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381647
hg191647
hg181647
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514838
Supporting Variants
SamplesNA19005
Known GenesCCL4L1, CCL4L2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2829249
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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