A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762989



Internal ID18961890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68788582..68795483hg38UCSC Ensembl
chr14:69255299..69262200hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg386902
hg196902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070226
Supporting Variants
SamplesKWP1
Known GenesZFP36L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762989
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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