A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765890



Internal ID18963981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99971362..99972463hg38UCSC Ensembl
chr14:100437699..100438800hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071169
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765890
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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