A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2917153



Internal ID15746706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:137492652..137494092hg38UCSC Ensembl
Innerchr5:136828341..136829781hg19UCSC Ensembl
Innerchr5:136856240..136857680hg18UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381441
hg191441
hg181441
Variant TypeCNV gain
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515019
Supporting Variants
SamplesNA19152
Known GenesSPOCK1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2917153
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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