A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070233



Internal ID19323325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95319862..95320363hg38UCSC Ensembl
chr14:95786199..95786700hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771887
SamplesKWP1
Known GenesCLMN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070233
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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