A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070209



Internal ID18970621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19434268..19434966hg38UCSC Ensembl
chr14:20020199..20020900hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38699
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763250
SamplesKWP1
Known GenesPOTEM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070209
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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