A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090102



Internal ID21267772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27742390..27746708hg38UCSC Ensembl
Innerchr10:28031319..28035637hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384319
hg194319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112285
Supporting Variants
Samplessample116
Known GenesMKX
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090102
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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