A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109093



Internal ID18918096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:59252427..59252494hg38UCSC Ensembl
Outerchr17:57329788..57329855hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954938
SamplesKWS1
Known GenesGDPD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109093
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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