A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138537



Internal ID19263273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:39262467..39262530hg38UCSC Ensembl
Outerchr17:37418720..37418783hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991123
SamplesKWS2
Known GenesFBXL20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138537
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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