A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953912



Internal ID16956099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:46291935..46327734hg38UCSC Ensembl
Outerchr17:44369301..44405100hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3835800
hg1935800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998758
SamplesBILGI_BIOE
Known GenesARL17A, ARL17B, LRRC37A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953912
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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