A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771752



Internal ID19305366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100239862..100240563hg38UCSC Ensembl
chr14:100706199..100706900hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070236
Supporting Variants
SamplesKWP1
Known GenesYY1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771752
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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