A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2772409



Internal ID15346520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275821..28280169hg38UCSC Ensembl
Innerchr10:28564750..28569098hg19UCSC Ensembl
Innerchr10:28604756..28609104hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384349
hg194349
hg184349
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514550
Supporting Variants
SamplesNA18857
Known GenesMPP7
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2772409
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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