A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765560



Internal ID19306699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105248462..105249063hg38UCSC Ensembl
chr14:105714799..105715400hg19UCSC 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 Variantsnsv1070669
Supporting Variants
SamplesKWP1
Known GenesBRF1, BTBD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765560
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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