A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952117



Internal ID16954304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:7014482..7028381hg38UCSC Ensembl
Outerchr17:6917801..6931700hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000236
SamplesBILGI_BIOE
Known GenesBCL6B, C17orf49, MIR195, MIR497, MIR497HG, RNASEK, RNASEK-C17orf49
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952117
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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