A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2897995



Internal ID15722026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196807868..196835004hg38UCSC Ensembl
Innerchr3:196534739..196561875hg19UCSC Ensembl
Innerchr3:198019136..198046272hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3827137
hg1927137
hg1827137
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515003
Supporting Variants
SamplesNA18997
Known GenesPAK2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2897995
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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