A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155492



Internal ID22085997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71901793..71916286hg38UCSC Ensembl
Outerchr17:71897542..71923977hg38UCSC Ensembl
Innerchr17:69897934..69912427hg19UCSC Ensembl
Outerchr17:69893683..69920118hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3826436
hg1926436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011872
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155492
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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