A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2771913



Internal ID15760693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34228814..34233154hg38UCSC Ensembl
Innerchr10:34517742..34522082hg19UCSC Ensembl
Innerchr10:34557748..34562088hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384341
hg194341
hg184341
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514552
Supporting Variants
SamplesNA19200
Known GenesPARD3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2771913
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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