A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772389



Internal ID18958230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101760362..101762063hg38UCSC Ensembl
chr14:102226699..102228400hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070658
Supporting Variants
SamplesKWP1
Known GenesPPP2R5C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772389
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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