A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155390



Internal ID22085895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18452078..18571332hg38UCSC Ensembl
Outerchr17:18416548..18592992hg38UCSC Ensembl
Innerchr17:18355392..18474646hg19UCSC Ensembl
Outerchr17:18319862..18496306hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38176445
hg19176445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n97
Supporting Variantsnssv4010167, nssv4010168
Samples
Known GenesCCDC144B, FAM106A, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155390
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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