A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765158



Internal ID19307496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70223366..70223524hg38UCSC Ensembl
chr14:70690083..70690241hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070643
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765158
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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