A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770861



Internal ID18959326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105419762..105420363hg38UCSC Ensembl
chr14:105886099..105886700hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070248
Supporting Variants
SamplesKWP1
Known GenesMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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