A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952086



Internal ID16954273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:150208..201609hg38UCSC Ensembl
Outerchr17:1..51400hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3851402
hg1951400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000205
SamplesBILGI_BIOE
Known GenesDOC2B, LOC100506371
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952086
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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