A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953877



Internal ID16956064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:31387283..31392082hg38UCSC Ensembl
Outerchr17:29714301..29719100hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998723
SamplesBILGI_BIOE
Known GenesRAB11FIP4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953877
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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