A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762583



Internal ID19305537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39291893..39292504hg38UCSC Ensembl
chr17:37448146..37448757hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072734
Supporting Variants
SamplesKWP1
Known GenesFBXL20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762583
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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