A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765714



Internal ID19308574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101560462..101561463hg38UCSC Ensembl
chr14:102026799..102027800hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071171
Supporting Variants
SamplesKWP1
Known GenesDIO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765714
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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